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"name": "Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops",
"description": "Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops\n\nIf you are looking for an ophthalmic solution that helps manage eye inflammation while providing soothing lubrication, Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops offer a comprehensive approach to ocular care. This combination formulation is designed to reduce inflammation, relieve discomfort, and maintain adequate moisture on the eye surface, making it a valuable option for patients experiencing irritation, postoperative inflammation, or dry eye symptoms.\n\nThe combination of Flurbiprofen Sodium, a non-steroidal anti-inflammatory drug (NSAID), and Hydroxypropyl Methylcellulose (HPMC), a trusted ocular lubricant, provides dual benefits. While Flurbiprofen Sodium helps control inflammation and pain, Hydroxypropyl Methylcellulose helps keep the eyes hydrated and comfortable by stabilizing the tear film.\n\nWidely used in ophthalmic practice, these eye drops are often prescribed before and after eye surgery, during inflammatory eye conditions, and in situations where lubrication and anti-inflammatory action are both required.\n\nThis detailed guide explains the uses, benefits, mechanism of action, dosage guidance, precautions, side effects, and reasons why buyers choose Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops.\n\nWhat Are Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops?\n\nFlurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops are a combination ophthalmic preparation containing:\n\nFlurbiprofen Sodium\n\nFlurbiprofen Sodium is a non-steroidal anti-inflammatory drug (NSAID) that helps reduce inflammation, pain, redness, and swelling in the eye. It works by inhibiting the production of inflammatory substances responsible for discomfort and tissue irritation.\n\nHydroxypropyl Methylcellulose (HPMC)\n\nHydroxypropyl Methylcellulose is a lubricating agent commonly used in artificial tears and ophthalmic solutions. It helps retain moisture on the eye surface, reducing dryness, irritation, and friction during blinking.\n\nTogether, these ingredients provide both therapeutic and comfort-enhancing benefits for various ocular conditions.\n\nHow Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops Work\n\nThe effectiveness of this ophthalmic solution comes from the combined actions of its two active components.\n\nFlurbiprofen Sodium Action\n\nFlurbiprofen Sodium works by:\n\nBlocking cyclooxygenase (COX) enzymes\nReducing prostaglandin production\nDecreasing inflammation and swelling\nMinimizing eye pain and discomfort\nPreventing inflammatory responses during eye procedures\nHydroxypropyl Methylcellulose Action\n\nHydroxypropyl Methylcellulose works by:\n\nForming a protective lubricating layer on the eye surface\nImproving tear film stability\nReducing dryness and irritation\nEnhancing eye comfort\nSupporting ocular surface protection\nDual Benefits\n\nThe combination helps:\n\nControl inflammation\nRelieve discomfort\nImprove lubrication\nSupport postoperative recovery\nPromote overall eye comfort\nUses of Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops\n1. Postoperative Eye Inflammation\n\nThese eye drops are frequently used after cataract surgery and other ophthalmic procedures to reduce inflammation and improve patient comfort.\n\n2. Prevention of Intraoperative Miosis\n\nFlurbiprofen Sodium may be used before certain eye surgeries to help maintain pupil dilation during the procedure.\n\n3. Ocular Inflammation\n\nThe medication helps manage inflammatory conditions affecting the eye surface and surrounding tissues.\n\n4. Eye Irritation and Discomfort\n\nThe lubricating action of Hydroxypropyl Methylcellulose helps soothe irritated eyes and improve comfort.\n\n5. Dry Eye Symptoms Associated with Inflammation\n\nPatients experiencing dryness alongside ocular inflammation may benefit from the combined anti-inflammatory and lubricating effects.\n\n6. Recovery After Eye Procedures\n\nThe formulation may support healing and comfort during the postoperative recovery period.\n\nKey Benefits of Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops\nEffective Inflammation Control\n\nFlurbiprofen Sodium helps reduce redness, swelling, and discomfort caused by inflammatory processes.\n\nEnhanced Eye Lubrication\n\nHydroxypropyl Methylcellulose provides long-lasting moisture and tear film support.\n\nImproved Post-Surgical Comfort\n\nThe combination is particularly beneficial for patients recovering from ophthalmic procedures.\n\nDual-Action Formula\n\nProvides both therapeutic anti-inflammatory effects and soothing lubrication in a single product.\n\nReduced Eye Irritation\n\nThe protective lubricating layer helps minimize friction and discomfort.\n\nSupports Ocular Surface Health\n\nMaintaining hydration and controlling inflammation contribute to healthier eye tissues.\n\nConvenient Administration\n\nCombining two functions in one ophthalmic solution simplifies treatment.\n\nWhy Buyers Choose Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops\n\nPatients and healthcare providers often prefer this combination because it addresses multiple eye care needs simultaneously.\n\nBuyer-Focused Advantages\nAnti-inflammatory and lubricating benefits in one product\nHelps reduce postoperative discomfort\nSupports eye hydration\nPromotes patient comfort\nSuitable for inflammatory eye conditions\nTrusted ophthalmic ingredients\nConvenient treatment option\nRecommended by eye care professionals\n\nThese benefits make Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops a valuable addition to ocular treatment plans.\n\nWho Can Benefit from Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops?\n\nThis ophthalmic solution may be suitable for:\n\nPatients recovering from eye surgery\nIndividuals experiencing ocular inflammation\nPeople with irritation associated with inflammatory eye conditions\nPatients requiring lubrication and inflammation control\nIndividuals suffering from postoperative eye discomfort\nPatients under ophthalmologist supervision for ocular treatment\n\nA healthcare professional should determine whether this medication is appropriate for your specific condition.\n\nHow to Use Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops\n\nAlways follow your doctor's instructions regarding dosage and frequency.\n\nGeneral Directions for Use\nWash your hands thoroughly before application.\nShake the bottle if instructed.\nTilt your head backward.\nPull down the lower eyelid gently.\nInstill the prescribed number of drops into the affected eye.\nClose your eyes for a few moments.\nAvoid touching the dropper tip to any surface.\nReplace the cap securely after use.\n\nUse the medication exactly as directed to achieve the best therapeutic results.\n\nImportant Precautions\n\nBefore using Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops, inform your healthcare provider if you:\n\nHave allergies to NSAIDs\nHave asthma sensitive to aspirin or NSAIDs\nWear contact lenses\nHave bleeding disorders\nAre pregnant or breastfeeding\nHave other eye diseases or infections\nAre using additional ophthalmic medications\n\nRegular follow-up may be necessary during prolonged treatment.\n\nPossible Side Effects of Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops\n\nLike all medications, side effects may occur in some individuals.\n\nCommon Side Effects\nTemporary burning sensation\nMild eye irritation\nTemporary blurred vision\nStinging after application\nIncreased tearing\nEye discomfort\nLess Common Side Effects\nEye redness\nSensitivity to light\nItching\nForeign body sensation\nRare but Serious Side Effects\n\nSeek immediate medical attention if you experience:\n\nSevere eye pain\nSignificant vision changes\nPersistent swelling\nSevere allergic reactions\nWorsening inflammation\n\nMost side effects are mild and temporary.\n\nStorage Instructions\n\nProper storage helps maintain product quality and effectiveness.\n\nRecommended Storage Guidelines\nStore at room temperature.\nProtect from direct sunlight.\nKeep the bottle tightly closed.\nAvoid excessive heat and moisture.\nDo not use after the expiration date.\nKeep out of reach of children.\n\nAlways follow the storage instructions provided on the packaging.\n\nFrequently Asked Questions\nWhat are Flurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops used for?\n\nThey are used to reduce eye inflammation while providing lubrication and comfort, particularly before and after eye surgery.\n\nCan these eye drops help with dry eyes?\n\nYes. The Hydroxypropyl Methylcellulose component helps improve moisture retention and tear film stability.\n\nAre these eye drops a steroid?\n\nNo. Flurbiprofen Sodium is a non-steroidal anti-inflammatory drug (NSAID).\n\nCan they be used after cataract surgery?\n\nYes. They are commonly prescribed as part of postoperative eye care under medical supervision.\n\nHow quickly do they work?\n\nMany patients experience symptom relief shortly after use, although full therapeutic benefits depend on the condition being treated.\n\nConclusion\n\nFlurbiprofen Sodium With Hydroxypropyl Methylcellulose Eye Drops offer an effective dual-action solution for managing eye inflammation and maintaining ocular comfort. By combining the anti-inflammatory properties of Flurbiprofen Sodium with the lubricating benefits of Hydroxypropyl Methylcellulose, these eye drops help reduce redness, swelling, irritation, and dryness while supporting overall eye health.\n\nWhether used for postoperative care, inflammatory eye conditions, or enhanced ocular lubrication, this ophthalmic formulation provides reliable relief and improved patient comfort. Its proven ingredients, convenient application, and comprehensive therapeutic benefits make it a preferred choice among ophthalmologists and patients seeking effective eye care solutions.",
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"description": "Moxifloxacin Eye Ointment 0.5% w/w\n\nIf you are searching for a reliable and effective treatment for bacterial eye infections, Moxifloxacin Eye Ointment 0.5% w/w is a trusted ophthalmic antibiotic formulation designed to provide targeted infection control and promote faster healing. This advanced eye ointment contains moxifloxacin, a broad-spectrum fluoroquinolone antibiotic that works against a wide range of bacteria responsible for ocular infections.\n\nBacterial eye infections can cause symptoms such as redness, irritation, swelling, discharge, pain, and discomfort. Without proper treatment, these infections may worsen and affect vision or overall eye health. Moxifloxacin Eye Ointment 0.5% w/w delivers the antibiotic directly to the site of infection, helping eliminate harmful bacteria while providing prolonged contact with the affected area.\n\nWhether prescribed for bacterial conjunctivitis, eyelid infections, corneal infections, or post-surgical infection prevention, Moxifloxacin Eye Ointment 0.5% w/w remains a preferred choice among ophthalmologists and patients seeking effective antibacterial eye care.\n\nWhat Is Moxifloxacin Eye Ointment 0.5% w/w?\n\nMoxifloxacin Eye Ointment 0.5% w/w is a topical ophthalmic antibiotic medication containing moxifloxacin as its active ingredient. Moxifloxacin belongs to the fluoroquinolone class of antibiotics and is known for its broad-spectrum antibacterial activity.\n\nThe ointment formulation allows the medication to remain in contact with the eye surface for a longer period compared to standard eye drops, ensuring sustained antibacterial action and improved therapeutic effectiveness.\n\nThis medication is commonly used for:\n\nBacterial conjunctivitis\nBacterial keratitis\nEyelid infections\nCorneal infections\nPost-operative infection prevention\nExternal ocular bacterial infections\nManagement of susceptible bacterial eye conditions\n\nMoxifloxacin Eye Ointment should only be used for bacterial infections and is not effective against viral, fungal, or allergic eye conditions.\n\nHow Moxifloxacin Eye Ointment 0.5% w/w Works\n\nThe effectiveness of Moxifloxacin Eye Ointment comes from its ability to eliminate infection-causing bacteria.\n\nMechanism of Action\n\nMoxifloxacin works by:\n\nInhibiting bacterial DNA replication\nBlocking bacterial growth and multiplication\nDestroying susceptible bacteria\nPreventing the spread of infection\nSupporting the natural healing process\n\nBy targeting essential bacterial enzymes required for survival, moxifloxacin effectively controls infection and helps restore eye health.\n\nThe ointment base also creates a protective layer over the eye surface, allowing prolonged antibiotic exposure and improved treatment outcomes.\n\nUses of Moxifloxacin Eye Ointment 0.5% w/w\n1. Bacterial Conjunctivitis\n\nOne of the most common uses of Moxifloxacin Eye Ointment is the treatment of bacterial conjunctivitis, often referred to as pink eye. It helps reduce redness, discharge, and irritation caused by bacterial infection.\n\n2. Bacterial Keratitis\n\nKeratitis is an infection of the cornea that can threaten vision if left untreated. Moxifloxacin helps eliminate the bacteria responsible and supports corneal healing.\n\n3. Eyelid Infections\n\nCertain bacterial infections affecting the eyelids can respond effectively to topical antibiotic therapy.\n\n4. Corneal Ulcers\n\nBacterial corneal ulcers require prompt treatment to prevent complications. Moxifloxacin provides direct antibacterial action at the site of infection.\n\n5. Post-Surgical Eye Care\n\nOphthalmologists may prescribe Moxifloxacin Eye Ointment after eye surgery to reduce the risk of bacterial infection during recovery.\n\n6. External Ocular Infections\n\nThe ointment can be used for various bacterial infections affecting the external structures of the eye.\n\nKey Benefits of Moxifloxacin Eye Ointment 0.5% w/w\nBroad-Spectrum Antibacterial Coverage\n\nMoxifloxacin is active against many bacteria commonly associated with eye infections.\n\nProlonged Contact Time\n\nThe ointment formulation remains on the eye surface longer than standard eye drops, enhancing therapeutic effectiveness.\n\nFast Infection Control\n\nThe medication begins working directly at the infection site to help reduce bacterial growth.\n\nSupports Faster Healing\n\nBy controlling infection, the ointment creates a favorable environment for tissue recovery.\n\nConvenient Night-Time Use\n\nMany patients find eye ointments particularly useful before bedtime due to their prolonged action.\n\nReduced Risk of Infection Spread\n\nEffective treatment helps prevent bacterial infection from worsening or spreading.\n\nTrusted Ophthalmic Antibiotic\n\nMoxifloxacin is widely used and recognized for its effectiveness in ophthalmic care.\n\nWhy Buyers Choose Moxifloxacin Eye Ointment 0.5% w/w\n\nPatients and healthcare providers often select Moxifloxacin Eye Ointment because of its proven ability to treat bacterial eye infections effectively.\n\nBuyer-Focused Advantages\nBroad-spectrum antibacterial activity\nLong-lasting ointment formulation\nDirect application to infected tissues\nTrusted antibiotic therapy\nEffective symptom relief\nSuitable for various bacterial eye infections\nSupports post-surgical eye care\nRecommended by ophthalmologists\n\nThese advantages make Moxifloxacin Eye Ointment 0.5% w/w a preferred choice for bacterial ocular infection management.\n\nWho Can Benefit from Moxifloxacin Eye Ointment 0.5% w/w?\n\nThis medication may be suitable for:\n\nAdults with bacterial eye infections\nPatients diagnosed with bacterial conjunctivitis\nIndividuals with bacterial corneal infections\nPatients recovering from eye surgery\nPeople experiencing bacterial eyelid infections\nIndividuals requiring topical antibiotic eye treatment\n\nA healthcare professional should determine whether this medication is appropriate for your condition.\n\nHow to Use Moxifloxacin Eye Ointment 0.5% w/w\n\nAlways follow your doctor's instructions regarding dosage and treatment duration.\n\nGeneral Directions for Use\nWash your hands thoroughly before application.\nTilt your head backward.\nPull down the lower eyelid gently.\nApply a small ribbon of ointment inside the lower eyelid.\nClose your eyes gently for a few moments.\nAvoid touching the tube tip to the eye or any surface.\nReplace the cap securely after use.\n\nTemporary blurred vision may occur immediately after application due to the ointment consistency.\n\nComplete the full prescribed course even if symptoms improve earlier.\n\nImportant Precautions\n\nBefore using Moxifloxacin Eye Ointment 0.5% w/w, inform your healthcare provider if you:\n\nHave allergies to moxifloxacin or other quinolone antibiotics\nWear contact lenses\nHave a history of severe allergic reactions\nAre pregnant or breastfeeding\nHave other eye disorders\nAre using additional eye medications\n\nAvoid wearing contact lenses during active eye infections unless instructed otherwise by your doctor.\n\nPossible Side Effects of Moxifloxacin Eye Ointment 0.5% w/w\n\nLike all medications, side effects may occur in some individuals.\n\nCommon Side Effects\nTemporary blurred vision\nMild eye irritation\nBurning sensation\nStinging after application\nIncreased tearing\nEye discomfort\nLess Common Side Effects\nEye redness\nItching\nDry eye sensation\nForeign body sensation\nSerious Side Effects\n\nSeek immediate medical attention if you experience:\n\nSevere eye pain\nSignificant swelling\nSudden vision changes\nSevere allergic reactions\nDifficulty breathing\nPersistent worsening of symptoms\n\nMost side effects are mild and resolve without intervention.\n\nStorage Instructions\n\nProper storage helps maintain product quality and effectiveness.\n\nRecommended Storage Conditions\nStore at room temperature.\nKeep away from direct sunlight.\nProtect from excessive heat and moisture.\nKeep the tube tightly closed.\nDo not use after the expiration date.\nKeep out of reach of children.\n\nAlways follow the storage instructions mentioned on the product packaging.\n\nFrequently Asked Questions\nWhat is Moxifloxacin Eye Ointment 0.5% w/w used for?\n\nIt is used to treat bacterial eye infections such as conjunctivitis, keratitis, and other susceptible ocular infections.\n\nIs it effective against viral eye infections?\n\nNo. Moxifloxacin is an antibiotic and works only against bacterial infections.\n\nHow long does treatment usually last?\n\nThe duration depends on the type and severity of the infection. Always follow your healthcare provider's recommendations.\n\nCan children use Moxifloxacin Eye Ointment?\n\nUse in children should only occur under medical supervision.\n\nCan I stop treatment once symptoms improve?\n\nNo. Completing the full prescribed course helps ensure complete infection control and reduces the risk of recurrence.\n\nConclusion\n\nMoxifloxacin Eye Ointment 0.5% w/w is a highly effective broad-spectrum ophthalmic antibiotic designed to treat bacterial eye infections and support rapid recovery. Its advanced ointment formulation provides prolonged contact with the eye surface, allowing sustained antibacterial action and enhanced treatment effectiveness.\n\nWhether used for bacterial conjunctivitis, keratitis, corneal infections, eyelid infections, or post-operative care, Moxifloxacin Eye Ointment 0.5% w/w offers reliable infection control and improved ocular comfort. Its proven clinical efficacy, convenient application, and broad-spectrum coverage make it a preferred choice among ophthalmologists and patients alike.",
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"name": "Sodium Hyaluronate Eye Drops",
"description": "Sodium Hyaluronate Eye Drops\n\nIf you are searching for an effective solution to relieve dry, irritated, burning, or tired eyes, Sodium Hyaluronate Eye Drops are among the most trusted ophthalmic lubricants recommended by eye care professionals. These eye drops are specially formulated to provide long-lasting hydration and protection to the ocular surface, helping maintain optimal eye comfort throughout the day.\n\nSodium Hyaluronate is a naturally occurring substance found in the human body. Its exceptional water-retaining capacity makes it highly effective in moisturizing the eyes and supporting the natural tear film. Whether your eye discomfort is caused by prolonged screen exposure, environmental factors, contact lens wear, or age-related tear deficiency, Sodium Hyaluronate Eye Drops can provide soothing and sustained relief.\n\nThis guide explores everything buyers need to know about Sodium Hyaluronate Eye Drops, including their uses, benefits, mechanism of action, proper usage, potential side effects, and why they are a preferred choice for dry eye management.\n\nWhat Are Sodium Hyaluronate Eye Drops?\n\nSodium Hyaluronate Eye Drops are lubricating ophthalmic solutions designed to hydrate and protect the surface of the eyes. The active ingredient, sodium hyaluronate, is a salt form of hyaluronic acid that possesses remarkable moisture-retaining properties.\n\nUnlike ordinary artificial tears, sodium hyaluronate forms a protective and stable lubricating layer over the cornea and conjunctiva. This helps reduce friction caused by blinking and environmental irritants while promoting natural healing of the ocular surface.\n\nThese eye drops are commonly used for:\n\nDry eye syndrome\nEye irritation\nBurning sensation in the eyes\nForeign body sensation\nEye fatigue due to screen use\nContact lens-related dryness\nPost-operative eye care\nEnvironmental eye stress\nHow Sodium Hyaluronate Eye Drops Work\n\nThe effectiveness of Sodium Hyaluronate Eye Drops lies in their unique viscoelastic properties. Sodium hyaluronate can attract and retain large amounts of water, creating a stable moisture reservoir on the eye surface.\n\nMechanism of Action\nHydrates the Ocular Surface\nRetains moisture and prevents excessive tear evaporation.\nStabilizes the Tear Film\nSupports the natural tear layer and enhances eye lubrication.\nProtects Corneal Cells\nForms a protective barrier against environmental irritants.\nReduces Friction During Blinking\nMinimizes discomfort and irritation associated with dry eyes.\nSupports Tissue Healing\nHelps maintain a healthy ocular environment for surface recovery.\n\nThis comprehensive action provides prolonged comfort and relief compared to many conventional eye lubricants.\n\nUses of Sodium Hyaluronate Eye Drops\n1. Dry Eye Syndrome\n\nOne of the primary uses of Sodium Hyaluronate Eye Drops is the management of dry eye disease. Individuals who produce insufficient tears or experience rapid tear evaporation can benefit significantly from regular use.\n\n2. Digital Eye Strain\n\nExtended screen exposure reduces blinking frequency, leading to eye dryness and fatigue. Sodium Hyaluronate Eye Drops help restore moisture and comfort during prolonged computer or mobile device use.\n\n3. Contact Lens Discomfort\n\nContact lens wearers often experience dryness and irritation. These eye drops provide additional lubrication that improves wearing comfort.\n\n4. Environmental Irritation\n\nDust, pollution, smoke, air conditioning, and windy environments can affect eye moisture levels. Sodium Hyaluronate Eye Drops help protect the eyes from these external stressors.\n\n5. Post-Surgical Eye Care\n\nMany ophthalmologists recommend Sodium Hyaluronate Eye Drops after procedures such as cataract surgery, LASIK, or other eye surgeries to promote healing and maintain comfort.\n\n6. Age-Related Dryness\n\nAs people age, natural tear production often decreases. Sodium Hyaluronate Eye Drops help compensate for reduced tear secretion and maintain ocular comfort.\n\nKey Benefits of Sodium Hyaluronate Eye Drops\nLong-Lasting Hydration\n\nThe superior water-binding ability of sodium hyaluronate provides prolonged eye moisture and reduces the need for frequent reapplication.\n\nImmediate Comfort\n\nUsers often experience rapid relief from dryness, burning, itching, and irritation after application.\n\nEnhanced Tear Film Stability\n\nSupports the natural tear layer, helping maintain consistent eye lubrication throughout the day.\n\nImproved Visual Comfort\n\nDry eyes can cause fluctuating vision and discomfort. Regular use helps improve overall visual quality and comfort.\n\nSuitable for Sensitive Eyes\n\nMany formulations are designed to be gentle and well tolerated by individuals with sensitive eyes.\n\nSupports Eye Surface Recovery\n\nHelps create an environment that supports natural healing and ocular surface protection.\n\nReduced Eye Fatigue\n\nParticularly beneficial for individuals who spend long hours working on computers, tablets, and smartphones.\n\nWho Can Benefit from Sodium Hyaluronate Eye Drops?\n\nSodium Hyaluronate Eye Drops are suitable for a wide range of users, including:\n\nOffice professionals\nStudents\nSenior citizens\nFrequent travelers\nContact lens users\nPeople exposed to air-conditioned environments\nIndividuals with chronic dry eye syndrome\nPatients recovering from eye surgery\nDrivers who spend extended hours on the road\n\nThese eye drops offer versatile relief for both occasional and chronic eye dryness.\n\nHow to Use Sodium Hyaluronate Eye Drops\n\nFor optimal results, follow these general application guidelines:\n\nWash your hands thoroughly.\nTilt your head backward.\nPull down the lower eyelid gently.\nInstill the recommended number of drops into the affected eye.\nClose your eyes for a few seconds.\nAvoid touching the dropper tip to any surface.\n\nAlways follow your healthcare professional's instructions regarding dosage and frequency of use.\n\nWhy Buyers Prefer Sodium Hyaluronate Eye Drops\n\nWhen purchasing eye lubricants, buyers often look for products that provide both immediate and long-lasting relief. Sodium Hyaluronate Eye Drops have become a preferred choice because they combine advanced hydration technology with excellent tolerability.\n\nReasons buyers choose these eye drops include:\n\nProven effectiveness for dry eyes\nLong-lasting lubrication\nEnhanced comfort during screen use\nSupport for contact lens wearers\nSuitable for daily use\nRecommended by eye care specialists\nEffective tear film stabilization\nReliable moisture retention\n\nThese benefits make Sodium Hyaluronate Eye Drops one of the most sought-after ocular lubricants in the market.\n\nPossible Side Effects of Sodium Hyaluronate Eye Drops\n\nSodium Hyaluronate Eye Drops are generally safe and well tolerated. However, some users may occasionally experience:\n\nMild temporary blurred vision\nSlight eye irritation\nTemporary stinging sensation\nMild redness\nIncreased tearing immediately after application\n\nThese effects are usually short-lived and resolve on their own. If severe discomfort, persistent redness, swelling, or allergic reactions occur, discontinue use and consult an eye care professional promptly.\n\nStorage Instructions\n\nTo maintain product quality and effectiveness:\n\nStore at room temperature.\nKeep away from direct sunlight and excessive heat.\nEnsure the bottle is tightly closed after use.\nDo not use after the expiry date.\nKeep out of reach of children.\n\nFollowing proper storage practices helps preserve the sterility and efficacy of the eye drops.\n\nConclusion\n\nSodium Hyaluronate Eye Drops are a highly effective solution for individuals seeking reliable relief from dry, irritated, and fatigued eyes. Their advanced moisture-retaining properties help stabilize the tear film, protect the ocular surface, and provide long-lasting comfort throughout the day.\n\nWhether you experience occasional dryness from screen exposure or require ongoing support for chronic dry eye syndrome, Sodium Hyaluronate Eye Drops offer a trusted and clinically preferred option. With benefits such as prolonged hydration, enhanced eye comfort, and support for ocular health, these eye drops remain an essential choice for maintaining clear, comfortable, and healthy eyes.\n\nFor best results, use Sodium Hyaluronate Eye Drops as directed by your healthcare professional and incorporate them into your daily eye care routine to enjoy sustained hydration and protection.",
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"description": "Dobelate Plus is a scientifically formulated supplement designed to support vascular health, enhance circulation, and promote overall wellness. Combining the powerful antioxidant properties of citrus bioflavonoids and vitamin C with the vascular-protective benefits of calcium dobesilate, this advanced formulation is particularly beneficial for individuals dealing with microcirculatory disorders, capillary fragility, and related conditions.\n\nWhat is Dobelate Plus?\n\nDobelate Plus is a combination tablet that brings together three key components:\n\nCitrus Bioflavonoids – Natural plant compounds known for their antioxidant and anti-inflammatory properties\nVitamin C (Ascorbic Acid)—Essential for immune function, collagen synthesis, and tissue repair\nCalcium Dobesilate – A vasoactive agent that improves blood flow and strengthens capillaries\n\nThis synergistic blend helps protect blood vessels, reduce oxidative stress, and improve circulation, making it especially useful in conditions like diabetic retinopathy, varicose veins, and hemorrhoids.\n\nKey Uses of Dobelate Plus\n\nDobelate Plus is widely used for the management and support of several health conditions related to poor blood circulation and vascular weakness:\n\n1. Diabetic Retinopathy\n\nOne of the primary uses of Dobelate Plus is in managing diabetic retinopathy. Calcium dobesilate helps reduce leakage from blood vessels in the retina and improves microcirculation, thereby protecting vision.\n\n2. Chronic Venous Insufficiency\n\nIt helps improve blood flow in the veins, reducing symptoms such as swelling, pain, heaviness, and cramps in the legs.\n\n3. Hemorrhoids (Piles)\n\nDobelate Plus strengthens blood vessels and reduces inflammation, providing relief from pain, bleeding, and discomfort associated with hemorrhoids.\n\n4. Varicose Veins\n\nBy enhancing vascular tone and reducing capillary permeability, it helps manage symptoms like swelling and visible enlarged veins.\n\n5. Capillary Fragility\n\nThe combination of Vitamin C and bioflavonoids strengthens capillary walls, reducing the risk of bruising and bleeding.\n\nKey Benefits of Dobelate Plus\n1. Improves Blood Circulation\n\nCalcium dobesilate enhances microcirculation, ensuring better oxygen and nutrient delivery to tissues.\n\n2. Strengthens Blood Vessels\n\nVitamin C and citrus bioflavonoids work together to reinforce capillary walls, reducing leakage and fragility.\n\n3. Powerful Antioxidant Protection\n\nCitrus bioflavonoids and vitamin C neutralize free radicals, protecting cells from oxidative damage.\n\n4. Reduces Inflammation\n\nThe anti-inflammatory properties help alleviate swelling and discomfort in vascular conditions.\n\n5. Supports Eye Health\n\nParticularly beneficial for people with diabetes, it helps maintain retinal health and reduces vision complications.\n\n6. Promotes Faster Healing\n\nVitamin C plays a crucial role in collagen formation, aiding tissue repair and recovery.\n\n7. Reduces Edema (Swelling)\n\nBy improving venous tone and reducing fluid leakage, it helps control swelling in legs and other areas.\n\nHow Does Dobelate Plus Work?\n\nDobelate Plus works through a multi-action mechanism:\n\nCalcium Dobesilate reduces blood viscosity and improves red blood cell flexibility, enhancing circulation. It also decreases capillary permeability, preventing leakage.\nVitamin C boosts collagen synthesis, which is essential for maintaining the integrity of blood vessels and skin.\nCitrus bioflavonoids enhance the effectiveness of vitamin C and provide additional antioxidant protection.\n\nTogether, these ingredients create a comprehensive approach to vascular health.\n\nRecommended Dosage\n\nThe dosage of Dobelate Plus should be taken as prescribed by a healthcare professional. Typically, it is taken orally with water after meals. Do not exceed the recommended dose without medical advice.\n\nPossible Side Effects\n\nDobelate Plus is generally well-tolerated when taken as directed. However, like any medication or supplement, it may cause some side effects in certain individuals:\n\nCommon Side Effects\nNausea or mild stomach discomfort\nDiarrhea\nSkin rash or itching\nRare but Serious Side Effects\nAllergic reactions (swelling, severe rash, difficulty breathing)\nFever or joint pain (in rare cases linked to calcium dobesilate)\n\nIf any unusual or severe symptoms occur, it is important to seek medical attention immediately.\n\nPrecautions and Warnings\nPregnancy & Breastfeeding: Consult a doctor before use\nKidney or Liver Conditions: Use with caution and under medical supervision\nAllergies: Avoid if allergic to any of the components\nDrug Interactions: Inform your doctor about any other medications you are taking\nWho Should Use Dobelate Plus?\n\nDobelate Plus is ideal for:\n\nIndividuals with diabetes experiencing eye complications\nPeople suffering from varicose veins or leg swelling\nPatients with hemorrhoids\nThose with weak capillaries or frequent bruising\nIndividuals looking to improve vascular and circulatory health\nStorage Instructions\nStore in a cool, dry place away from direct sunlight\nKeep out of reach of children\nDo not use after the expiration date\nConclusion\n\nDobelate Plus is a comprehensive vascular health supplement that combines the benefits of citrus bioflavonoids, vitamin C, and calcium dobesilate to support healthy blood circulation and strengthen blood vessels. Its multi-functional formula not only helps manage conditions like diabetic retinopathy, varicose veins, and hemorrhoids but also provides powerful antioxidant protection and promotes overall wellness.",
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"name": "Cinnarizine and Domperidone Tablets ",
"description": "CLANARIZINE DOM represents an advanced pharmaceutical combination that brings together two potent therapeutic agents—Cinnarizine and Domperidone—in a single convenient tablet formulation. This innovative combination medication addresses multiple aspects of vestibular disorders, motion sickness, and associated nausea and vomiting, providing comprehensive relief for patients suffering from these debilitating conditions. Manufactured under stringent quality control standards, CLANARIZINE DOM offers a synergistic approach to managing symptoms that significantly impact quality of life and daily functioning.The combination of Cinnarizine and Domperidone in CLANARIZINE DOM is based on sound pharmacological principles. While Cinnarizine works primarily on the vestibular system to reduce dizziness and vertigo, Domperidone acts as an effective antiemetic to control nausea and vomiting. Together, these two active ingredients provide more comprehensive symptom control than either agent alone, making CLANARIZINE DOM an excellent choice for patients experiencing vestibular disturbances accompanied by gastrointestinal symptoms.This combination therapy is particularly valuable because vertigo, dizziness, and motion sickness are frequently accompanied by nausea and vomiting. Patients suffering from these conditions often find that addressing only one aspect of their symptoms provides insufficient relief. CLANARIZINE DOM's dual-action formula tackles both the underlying vestibular dysfunction and the accompanying gastrointestinal distress, offering patients a more complete therapeutic solution that improves both comfort and functional capacity.Understanding the Active IngredientsCinnarizine is a calcium channel blocker with specific antihistaminic and vestibular suppressant properties. Unlike systemic calcium channel blockers used for cardiovascular conditions, Cinnarizine selectively acts on the blood vessels in the inner ear and brain, improving blood flow to these areas. This enhanced circulation helps reduce the frequency and severity of vertigo attacks while also preventing motion sickness. Cinnarizine also possesses mild antihistaminic effects that contribute to its anti-nausea properties, though this is not its primary mechanism of action.The medication works by blocking calcium channels in the vestibular system, which helps stabilize the sensory organs responsible for balance. By reducing the excessive stimulation of the vestibular apparatus, Cinnarizine decreases the sensation of spinning or imbalance that characterizes vertigo. Additionally, its vasodilatory effects improve microcirculation in the inner ear, which can be beneficial for conditions where reduced blood flow contributes to symptoms.Domperidone is a peripheral dopamine antagonist that acts primarily as a prokinetic and antiemetic agent. Unlike some antiemetic medications that cross the blood-brain barrier and cause sedation or extrapyramidal side effects, Domperidone works predominantly in the peripheral nervous system. It blocks dopamine receptors in the chemoreceptor trigger zone (CTZ) located outside the blood-brain barrier, effectively preventing nausea and vomiting without causing significant central nervous system effects.Domperidone also enhances gastrointestinal motility by promoting coordinated contractions of the stomach and upper small intestine. This prokinetic effect helps empty the stomach more efficiently, reducing feelings of fullness, bloating, and discomfort that often accompany vestibular disorders. By accelerating gastric emptying, Domperidone also reduces the likelihood of gastroesophageal reflux, which can exacerbate nausea in some patients.The combination of these two medications in CLANARIZINE DOM creates a complementary therapeutic effect. While Cinnarizine addresses the vestibular component of dizziness and vertigo, Domperidone manages the gastrointestinal symptoms that frequently accompany these conditions. This dual approach provides more comprehensive symptom relief and improves overall treatment outcomes compared to monotherapy with either agent alone.Clinical Applications and UsesCLANARIZINE DOM is indicated for a wide range of conditions characterized by vertigo, dizziness, and associated nausea. Understanding these clinical applications helps healthcare providers select appropriate candidates for this combination therapy.Vestibular Disorders: The primary indication for CLANARIZINE DOM includes various vestibular disorders that cause vertigo and imbalance. These conditions include Ménière's disease, benign paroxysmal positional vertigo (BPPV), vestibular neuritis, and labyrinthitis. Patients with these disorders experience episodes of spinning sensation, loss of balance, and often severe nausea. CLANARIZINE DOM helps reduce the frequency and intensity of vertigo attacks while controlling the accompanying gastrointestinal symptoms.Motion Sickness: CLANARIZINE DOM is highly effective for preventing and treating motion sickness, whether related to travel by car, boat, airplane, or amusement park rides. The medication can be taken prophylactically before travel or at the onset of symptoms. The combination is particularly useful for individuals who experience severe nausea and vomiting with motion sickness, as Domperidone provides powerful antiemetic effects that complement Cinnarizine's anti-motion-sickness properties.Migraine-Associated Vertigo: Many patients with migraines experience vestibular symptoms, including dizziness, vertigo, and motion sensitivity, either during migraine attacks or as independent episodes. CLANARIZINE DOM can help manage these vestibular manifestations of migraine, reducing both the vertigo and the nausea that often accompany migraine headaches.Post-Concussion Syndrome: Following head injuries, some patients develop persistent dizziness, balance problems, and nausea as part of post-concussion syndrome. CLANARIZINE DOM may provide symptomatic relief for these patients during their recovery period, though it should be used as part of a comprehensive treatment approach that includes rest, gradual return to activities, and vestibular rehabilitation when appropriate.Cerebrovascular Insufficiency: In older adults with reduced blood flow to the brain, symptoms such as dizziness, vertigo, tinnitus (ringing in the ears), and cognitive difficulties may develop. Cinnarizine's vasodilatory properties can improve cerebral circulation, potentially reducing these symptoms. The addition of Domperidone helps manage any associated nausea.Radiation-Induced or Chemotherapy-Induced Nausea: While not a primary indication, some healthcare providers use CLANARIZINE DOM as adjunctive therapy for patients undergoing cancer treatment who experience both nausea and dizziness. Domperidone's strong antiemetic properties are particularly valuable in this context.Key Benefits of CLANARIZINE DOMThe unique combination of Cinnarizine and Domperidone in CLANARIZINE DOM offers numerous advantages that make it a preferred choice for managing vestibular disorders and associated symptoms.Comprehensive Symptom Control: The primary benefit of CLANARIZINE DOM is its ability to address multiple symptoms simultaneously. Rather than requiring patients to take separate medications for vertigo and nausea, this combination provides unified treatment in a single tablet. This comprehensive approach improves symptom control across the full spectrum of vestibular disorder manifestations, from the spinning sensation to the gastrointestinal distress that often accompanies it.Improved Patient Compliance: Taking multiple medications can be burdensome, particularly for patients who feel dizzy or nauseated. CLANARIZINE DOM simplifies the treatment regimen by combining two medications in one tablet, making it easier for patients to adhere to their prescribed therapy. Better compliance translates to better outcomes, as consistent medication use is essential for managing chronic vestibular conditions.Synergistic Therapeutic Effects: The combination of Cinnarizine and Domperidone creates synergistic effects that enhance overall efficacy. While Cinnarizine reduces vestibular stimulation and improves inner ear blood flow, Domperidone prevents nausea and promotes gastric emptying. This dual action addresses both the cause and consequences of vestibular dysfunction, providing more complete relief than either medication alone.Reduced Central Nervous System Side Effects: Because Domperidone works primarily in the peripheral nervous system rather than crossing the blood-brain barrier extensively, CLANARIZINE DOM causes less sedation and fewer cognitive effects compared to some alternative antiemetic medications. This allows patients to maintain better alertness and function during treatment, which is particularly important for those who need to continue working or performing daily activities.Enhanced Quality of Life: Vertigo and chronic dizziness significantly impair quality of life, limiting mobility, social interactions, and occupational functioning. The nausea and vomiting that accompany these conditions add another layer of disability. By effectively controlling both vestibular and gastrointestinal symptoms, CLANARIZINE DOM helps restore patients' ability to engage in normal activities, improving overall life satisfaction and functional independence.Fast Onset of Action: CLANARIZINE DOM provides relatively rapid symptom relief, with many patients experiencing improvement within 30 minutes to 2 hours after taking the medication. This quick onset is particularly valuable for acute episodes of vertigo or when taking the medication prophylactically before situations that might trigger motion sickness.Suitable for Long-Term Use: For patients with chronic vestibular disorders requiring ongoing treatment, CLANARIZINE DOM is generally safe for extended use when properly monitored by a healthcare provider. The medication maintains its effectiveness over time without significant tolerance development, making it suitable for long-term symptom management.Improved Gastric Emptying: The prokinetic effects of Domperidone benefit not only nausea but also other gastrointestinal symptoms such as early satiety, bloating, and upper abdominal discomfort. Patients with vestibular disorders often develop gastroparesis or delayed gastric emptying secondary to their condition, and Domperidone addresses this issue effectively.Vascular Benefits: Cinnarizine's ability to improve blood flow to the inner ear and brain provides additional benefits beyond symptom control. Enhanced microcirculation may support healing and recovery in conditions where vascular insufficiency contributes to vestibular dysfunction.Side Effects and Safety ConsiderationsLike all medications, CLANARIZINE DOM can cause side effects, though not everyone experiences them. Understanding potential adverse effects helps patients recognize when to seek medical attention and allows healthcare providers to monitor therapy appropriately.Common Side Effects:The most frequently reported side effect of CLANARIZINE DOM is drowsiness or sedation, occurring in approximately 10-20% of patients. This effect is primarily attributable to Cinnarizine's antihistaminic properties. Patients should avoid driving or operating machinery until they know how the medication affects them. Taking the medication at bedtime can minimize daytime drowsiness for some patients.Dry mouth is another common side effect, affecting roughly 10-15% of patients. This occurs due to anticholinergic effects and can be managed by sipping water frequently, chewing sugar-free gum, or using saliva substitutes if severe. Maintaining good oral hygiene is important to prevent dental problems associated with reduced saliva production.Mild gastrointestinal symptoms, including constipation, abdominal discomfort, or changes in bowel habits, may occur. While Domperidone promotes gastric emptying, it can occasionally alter bowel motility. These effects are usually mild and resolve with continued use or dose adjustment.",
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"description": "MIRTAZPRIME 30 is a pharmaceutical formulation containing Mirtazapine 30mg as per Indian Pharmacopoeia (IP) standards. This prescription medication belongs to a class of drugs known as tetracyclic antidepressants and represents an advanced therapeutic option for individuals struggling with major depressive disorder and related mental health conditions. Manufactured under stringent quality control measures, MIRTAZPRIME 30 offers patients a reliable and effective solution for managing depression while also addressing associated symptoms such as insomnia and anxiety.\nMirtazapine, the active pharmaceutical ingredient in MIRTAZPRIME 30, works through a unique dual mechanism that distinguishes it from other antidepressants. Unlike selective serotonin reuptake inhibitors (SSRIs), mirtazapine enhances the release of both norepinephrine and serotonin in the brain by blocking specific receptors. This innovative approach not only helps alleviate depressive symptoms but also provides sedative effects that can be particularly beneficial for patients experiencing sleep disturbances alongside depression.\nTherapeutic Uses and Applications\nMIRTAZPRIME 30 is primarily indicated for the treatment of major depressive disorder (MDD), a serious mental health condition characterized by persistent feelings of sadness, hopelessness, and loss of interest in daily activities. The medication has demonstrated significant efficacy in clinical trials, showing improvement in mood, energy levels, and overall quality of life for patients suffering from depression.\nBeyond its primary indication, healthcare providers may prescribe MIRTAZPRIME 30 for various off-label uses based on clinical judgment and patient needs. The medication has shown promise in managing generalized anxiety disorder, where excessive worry and tension interfere with daily functioning. Its sedative properties make it particularly valuable for patients experiencing insomnia related to depression or anxiety, as it can help restore healthy sleep patterns without the need for additional sleep medications.\nThe 30mg dosage strength represents a therapeutic level commonly prescribed for maintenance treatment after initial dose titration. Patients typically begin with lower doses and gradually increase to 30mg as their body adjusts to the medication and their symptoms require more robust management. This dosage provides an optimal balance between therapeutic efficacy and side effect management for many individuals.\nMIRTAZPRIME 30 may also be considered for patients who have not responded adequately to other antidepressant therapies, offering an alternative mechanism of action that can break through treatment-resistant depression. Additionally, its appetite-stimulating effects can be beneficial for patients experiencing significant weight loss due to depression or other medical conditions.\nKey Benefits and Therapeutic Advantages\nThe benefits of MIRTAZPRIME 30 extend beyond simple symptom relief, offering patients a multifaceted approach to mental health recovery. One of the most significant advantages is its relatively rapid onset of action compared to many other antidepressants. While most SSRIs require several weeks to demonstrate meaningful clinical improvement, patients taking mirtazapine often experience some relief from symptoms within one to two weeks, with continued improvement over subsequent weeks.\nThe dual neurotransmitter action of MIRTAZPRIME 30 provides comprehensive coverage of depressive symptoms. By enhancing both serotonergic and noradrenergic neurotransmission, the medication addresses the complex neurochemical imbalances underlying depression more thoroughly than single-mechanism antidepressants. This broader action can result in more complete symptom resolution and better overall outcomes.\nSleep improvement represents another crucial benefit of MIRTAZPRIME 30. The medication's sedative properties, particularly pronounced at lower doses, help patients fall asleep faster and enjoy more restorative sleep throughout the night. This is especially valuable since sleep disturbances are both a symptom and an exacerbating factor in depression. Better sleep quality contributes to improved daytime functioning, energy levels, and emotional regulation.\nUnlike many antidepressants that commonly cause sexual dysfunction, MIRTAZPRIME 30 has a relatively favorable profile in this regard. The medication is less likely to interfere with sexual function, making it an attractive option for patients who have experienced these troublesome side effects with other antidepressants. This characteristic can significantly improve treatment adherence and quality of life.\nThe appetite-stimulating effect, while considered a side effect by some, can be therapeutically beneficial for patients experiencing significant weight loss or poor appetite due to depression. MIRTAZPRIME 30 can help restore healthy eating patterns and reverse the physical decline that often accompanies severe depressive episodes.\nFurthermore, MIRTAZPRIME 30 does not typically cause the gastrointestinal side effects commonly associated with SSRI antidepressants, such as nausea, diarrhea, or stomach upset. This improved gastrointestinal tolerability enhances patient comfort and compliance with treatment regimens.\nPotential Side Effects and Safety Considerations\nWhile MIRTAZPRIME 30 offers numerous therapeutic benefits, patients should be aware of potential side effects that may occur during treatment. Understanding these effects helps patients make informed decisions and enables early identification of any concerning symptoms requiring medical attention.\nThe most commonly reported side effect is drowsiness or sedation, particularly during the initial weeks of treatment. This effect is typically most pronounced during the first few hours after taking the medication, which is why it's generally recommended for evening administration. Patients should exercise caution when driving, operating machinery, or engaging in activities requiring alertness until they understand how the medication affects them personally.\nIncreased appetite and weight gain represent another frequent side effect of MIRTAZPRIME 30. While beneficial for some patients, others may find this effect undesirable. Weight gain typically ranges from moderate to significant and appears to be dose-related. Patients concerned about weight should discuss dietary strategies and exercise plans with their healthcare provider.\nDry mouth is a common anticholinergic side effect that can cause discomfort but is generally manageable through increased fluid intake, sugar-free gum or candy, and good oral hygiene practices. Some patients may also experience dizziness, particularly when standing up quickly, due to the medication's effects on blood pressure regulation.\nConstipation may occur in some patients and can usually be managed through dietary modifications, increased fiber intake, adequate hydration, and regular physical activity. Less commonly, patients might experience confusion, abnormal dreams, or changes in thinking, particularly in older adults who may be more sensitive to the medication's effects.\nSerious side effects, while rare, require immediate medical attention. These include signs of allergic reactions such as rash, itching, swelling, severe dizziness, or difficulty breathing. Agranulocytosis, a dangerous decrease in white blood cells, is an extremely rare but serious complication that manifests as fever, sore throat, or signs of infection. Any unexplained fever or signs of infection should prompt immediate contact with a healthcare provider.\nSerotonin syndrome is another rare but potentially life-threatening condition that can occur when mirtazapine is combined with other medications affecting serotonin levels. Symptoms include agitation, hallucinations, rapid heartbeat, fever, excessive sweating, muscle stiffness, or coordination problems. Patients should inform their healthcare provider about all medications and supplements they are taking to avoid dangerous interactions.\nAbrupt discontinuation of MIRTAZPRIME 30 can lead to withdrawal symptoms, including nausea, anxiety, irritability, and flu-like symptoms. Therefore, any decision to stop the medication should be made in consultation with a healthcare provider who can develop an appropriate tapering schedule.\nImportant Usage Guidelines\nMIRTAZPRIME 30 should always be taken exactly as prescribed by a qualified healthcare professional. The medication is typically administered once daily, preferably in the evening before bedtime due to its sedative effects. Tablets should be swallowed whole with water and can be taken with or without food, though taking them with food may help reduce any stomach upset.\nConsistency in timing is important for maintaining stable blood levels of the medication and optimizing therapeutic effects. Patients should try to take their dose at approximately the same time each evening. If a dose is missed, it should be taken as soon as remembered unless it's close to the time for the next scheduled dose, in which case the missed dose should be skipped rather than doubling up.\nThe full therapeutic benefits of MIRTAZPRIME 30 may take several weeks to manifest. Patients should continue taking the medication as prescribed even if they don't feel immediate improvement. Premature discontinuation is a common reason for treatment failure in depression management.\nRegular follow-up appointments with the prescribing physician are essential for monitoring treatment response, adjusting dosages if necessary, and screening for potential side effects. Patients should maintain open communication with their healthcare team about their symptoms, concerns, and any changes in their condition.\nConclusion\nMIRTAZPRIME 30 represents a valuable therapeutic option in the comprehensive management of major depressive disorder and related conditions. Its unique mechanism of action, combining enhanced noradrenergic and serotonergic neurotransmission with sedative and appetite-stimulating properties, offers distinct advantages for carefully selected patients. The medication's ability to improve both mood symptoms and sleep disturbances makes it particularly useful for patients experiencing depression accompanied by insomnia.\nThe relatively favorable side effect profile, particularly regarding sexual function and gastrointestinal tolerability, enhances patient acceptance and adherence to treatment. While potential side effects such as sedation, increased appetite, and weight gain require monitoring and management, many patients find these effects tolerable compared to the debilitating symptoms of untreated depression.\nSuccess with MIRTAZPRIME 30, as with any antidepressant therapy, depends on proper patient selection, appropriate dosing, regular monitoring, and a comprehensive treatment approach that may include psychotherapy, lifestyle modifications, and social support alongside pharmacological intervention. Patients should work closely with their healthcare providers to optimize treatment outcomes and maintain long-term mental health wellness.\nThe decision to use MIRTAZPRIME 30 should always be made collaboratively between patient and physician, considering individual symptoms, treatment history, coexisting medical conditions, and personal preferences. With proper use under medical supervision, MIRTAZPRIME 30 can be an effective tool in helping patients reclaim their lives from the devastating effects of depression and move toward recovery and renewed well-being.",
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"description": "Eligolux200 contains 200 mg of elagolix per tablet and is manufactured by Steris Healthcare Pvt Ltd in India as a prescription medication in packs of 3x10 tablets. Elagolix acts as a potent gonadotropin-releasing hormone (GnRH) receptor antagonist, binding competitively to GnRH receptors in the pituitary gland to rapidly reduce estrogen and progesterone levels without the initial flare-\nup seen in agonists. This mechanism starves endometrial-like tissue outside the uterus of hormonal stimulation, shrinking lesions and easing inflammation.\n\nAdminister Eligolux200 orally, swallowed whole with water, with or without food, typically starting within 7 days of menstrual onset. Standard dosing for severe cases involves 200mg twice daily for up to 6 months, or 150mg once daily extended to 24 months, adjusted by physicians based on tolerance and response. Store in a cool, dry place away from moisture and light, keeping out of children's reach.\n\nPrimary Uses\nEligolux200 targets moderate to severe endometriosis-associated pain, including dysmenorrhea (painful periods), nonmenstrual pelvic pain, and dyspareunia (painful intercourse). Endometriosis affects millions globally, causing tissue similar to the uterine lining to grow ectopically, leading to chronic inflammation, adhesions, and scarring. By dosing flexibly, Eligolux200 suits patients needing stronger suppression for intense symptoms, reducing reliance on opioids or surgery.\n\nClinical trials like Elaris EM-I and EM-II showed 75% dysmenorrhea reduction and 50-60% nonmenstrual pain relief at 6-12 months. It also curbs heavy menstrual bleeding in uterine fibroids, offering dual benefits for overlapping conditions. Physicians prescribe it when first-line NSAIDs or oral contraceptives fail, prioritizing non-invasive symptom control.\n\n\nKey Benefits\nEligolix in Eligolux200 delivers rapid pain relief, with significant improvements in daily pain scales within 3 months versus placebo. Women report 47% better composite pelvic pain scores, enhancing daily activities, work productivity, and intimacy. Quality-of-life metrics improve consistently over 24 weeks, including reduced fatigue and better emotional well-being.\n\n\nUnlike injectables, its oral form and dose-dependent estrogen suppression allow titration—lower doses minimize hypoestrogenic effects while higher 200mg dosing tackles severe pain. Studies confirm amenorrhea in 25% of users early on, slashing bleeding days by up to 50%. Long-term data up to 12 months with add-back therapy sustains efficacy, preserving bone health better than monotherapy. Patients regain control, avoiding invasive laparoscopies and reclaiming normalcy.\n\n\nBenefit\tEvidence from Trials'\tImpact on Patients\nDysmenorrhea Reduction:\t75% at 6 months \n\tFewer missed workdays\nNonmenstrual Pain Relief:\t50-60% improvement \n\tEnhanced mobility\nBleeding Control:\t14% bleeding days vs. 24% baseline \n\tImproved hygiene, anemia prevention\nQuality of Life\tSustained over 24 weeks \n\tBetter sleep, relationships\nPotential Side Effects\nCommon side effects of Eligolux200 mirror hypoestrogenic states: hot flashes, night sweats, headache, and nausea, each affecting about 10% of users. These often lessen as the body adjusts, with 69.5% overall adverse event rate over 24 weeks, mostly mild. Mood changes like irritability or depression occur less commonly, warranting mood monitoring.\n\n\nBone mineral density (BMD) loss poses a key concern—200mg twice daily causes -1.5% to -2.4% drops at lumbar spine and hip after 6 months, attenuated with calcium/vitamin D or add-back therapy. Rare serious risks include suicidal thoughts, liver enzyme elevations, or allergic reactions like anaphylaxis. Discontinuation due to events stays low at 4-12%. No deaths are linked directly to treatment in trials.\n\n\nSide Effect Category\tFrequency\tManagement\nVasomotor (Hot Flashes)\t9.9-10% \n\tLifestyle cooling, dose adjustment\nNeurologic (Headache)\t9.9% \n\tHydration, analgesics\nBone Loss\tUp to 2.4% at 6 months \n\tDEXA scans, supplements\nMood Changes\tLess common \n\tPsychiatric screening\nPrecautions and Contraindications\nAvoid Eligolux200 in pregnancy (risk of early loss), known osteoporosis, severe hepatic impairment, or with strong OATP1B1 inhibitors like cyclosporine or gemfibrozil. Women of childbearing age need effective non-hormonal contraception during and 28 days post-therapy, as it impairs recognition of pregnancy via amenorrhea. Not for pediatrics under 18 or geriatrics lacking data.\n\nScreen for depression history, liver function, and BMD before starting; monitor quarterly. Drug interactions abound with rifampin (reduces levels) or over 50 others like clarithromycin—inform physicians fully. Breastfeeding lacks safety data; weigh risks. Regular blood/urine tests track efficacy and safety.\n\n\nDosage Guidelines\nInitiate Eligolux200 at 150mg daily for milder cases, escalating to 200mg BID for dyspareunia or severe pain, max 6 months at higher dose. Miss a dose? Take promptly unless near the next; never double. Duration caps at 24 months total, with liver-adjusted lower dosing. Pair with add-back for extended use to curb BMD loss.\n\n\nPhysicians tailor based on response: 74-77% complete 6-month trials. Swallow intact; no crushing.\n\n\nClinical Evidence\nPhase III trials (Elaris EM-I/II) randomized 1689 women, proving both doses superior to placebo for co-primary endpoints of dysmenorrhea and nonmenstrual pain. Open-label extensions to 24 weeks maintained gains. A 12-month study with add-back showed persistent relief and <1% additional BMD loss versus placebo. Real-world use echoes this, positioning Eligolix as first oral GnRH antagonist approved for endometriosis.\n\n\nVersus relugolix, Eligolix offers comparable pelvic pain reduction with adjustable dosing. Indian brands like Eligolux200 align with global standards.\n\n\nConclusion\nEligolux200 transforms endometriosis management, delivering substantial pain relief and functional gains through precise hormonal control. Balancing robust benefits against manageable risks like BMD monitoring empowers women toward symptom-free lives. Consult healthcare providers for personalized integration into care plans.\n",
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"description": "Ketoconazole & Coal Tar Solution Shampoo stands out as a powerful medicated formulation designed to combat persistent scalp issues like dandruff, seborrheic dermatitis, and psoriasis. This dual-action shampoo combines the antifungal prowess of ketoconazole with the soothing, keratolytic properties of coal tar, making it an essential tool for restoring scalp balance and promoting healthier hair growth. Ideal for those frustrated by itching, flaking, and irritation, this shampoo targets the root causes while gently cleansing the hair.\n\nRegular use of Ketoconazole & Coal Tar Solution Shampoo helps regulate excessive oil production, reduces inflammation, and prevents the recurrence of scalp conditions. Whether you're dealing with chronic dandruff or more severe dermatological challenges, this product offers visible relief within weeks, enhancing overall scalp comfort and confidence. Available from trusted providers like Steris Healthcare, it fits seamlessly into daily hair care routines for long-term results.\n\nUses of Ketoconazole & Coal Tar Solution Shampoo\nThis medicated shampoo excels in treating a range of scalp disorders driven by fungal overgrowth or rapid skin cell turnover. Primarily, it addresses dandruff by eliminating the Malassezia fungus responsible for flaking and itching. For seborrheic dermatitis, it reduces oily, red patches on the scalp, providing targeted antifungal action alongside anti-inflammatory relief.\n\nBeyond dandruff, Ketoconazole & Coal Tar Solution Shampoo proves effective against psoriasis, where coal tar slows excessive skin cell production to minimize thick, scaly plaques. It also aids in managing mild eczema or contact dermatitis on the scalp by soothing irritation and preventing secondary infections. Dermatologists often recommend it for maintenance therapy after initial treatment, ensuring sustained scalp health without daily use.\n\nUsers with oily scalps or those in humid climates find it particularly beneficial, as it controls sebum buildup that exacerbates these conditions. Apply it to wet hair, massage into the scalp, leave for 3-5 minutes, and rinse thoroughly—typically 2-3 times weekly or as prescribed. This routine not only cleanses but also fortifies the scalp barrier against environmental stressors.\n\nKey Benefits of Ketoconazole & Coal Tar Solution Shampoo\nThe synergistic blend in this shampoo delivers multifaceted benefits, starting with potent antifungal activity from ketoconazole, which disrupts ergosterol synthesis in fungal cell membranes, halting their growth. This leads to rapid reduction in itching and flaking, often noticeable after the first few uses.\n\nCoal tar complements this by acting as a keratolytic agent, breaking down thick scales and reducing inflammation through its anti-pruritic properties. Together, they promote a balanced scalp microbiome, regulate oil glands, and improve hair texture by preventing buildup that causes breakage. Long-term benefits include fewer flare-ups, enhanced hair shine, and reduced need for additional treatments.\n\nRapid Symptom Relief: Alleviates itching, redness, and scaling within 1-4 weeks of consistent use.\n\nPrevents Recurrence: Maintains scalp health with prophylactic application, ideal for chronic conditions.\n\nGentle on Hair: Cleanses without stripping natural oils, suitable for all hair types including colored or treated hair.\n\nAnti-Inflammatory Action: Soothes irritated skin, minimizing discomfort from psoriasis or dermatitis.\n\nConvenient Topical Use: Easy-to-apply shampoo format encourages adherence over lotions or creams.\n\nClinical insights highlight its efficacy in improving quality of life, with many users reporting flake-free scalps and boosted confidence. For those with sensitive skin, the formulation balances potency with gentleness, making it a go-to for family use under medical guidance.\n\nSide Effects of Ketoconazole & Coal Tar Solution Shampoo\nWhile generally well-tolerated, Ketoconazole & Coal Tar Solution Shampoo may cause mild, transient side effects as the scalp adjusts. Common reactions include temporary dryness, mild irritation, or redness at the application site, which often resolve with continued use or moisturizing follow-up.\n\nSome individuals experience scalp oiliness, stinging, or burning sensation initially, particularly if left on longer than recommended. Hair discoloration or unusual texture changes can occur rarely, especially with coal tar's photosensitizing effects—avoid direct sunlight post-application. Allergic responses like rash or swelling warrant immediate discontinuation.\n\nSerious side effects are uncommon but include severe dermatitis, persistent itching, or folliculitis. Those with coal tar sensitivity or open wounds should avoid it. Always patch-test first and consult a dermatologist if symptoms worsen. Between treatments, pair with a mild conditioner to counteract dryness.\n\nPregnant or breastfeeding individuals need medical advice due to limited safety data. Avoid eye contact; rinse thoroughly if it occurs. Monitoring ensures safe use, with most side effects manageable through proper application.\n\nConclusion\nKetoconazole & Coal Tar Solution Shampoo emerges as a reliable, dual-action powerhouse for tackling dandruff, seborrheic dermatitis, psoriasis, and related scalp woes, delivering lasting relief through antifungal and keratolytic mechanisms. Its key benefits—quick symptom control, recurrence prevention, and scalp revitalization—outweigh minor side effects for most users, fostering healthier hair and skin with consistent use. Embrace this shampoo as part of your routine for flake-free confidence; consult healthcare professionals for personalized advice from Steris Healthcare or similar trusted sources. Prioritize scalp health today for a vibrant, itch-free tomorrow.",
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"name": "Nicorandil Tablets 5mg",
"description": "Nicorandil Tablets 5 mg is a vasodilatory anti-anginal medication widely prescribed for the management and prevention of angina pectoris (chest pain) associated with coronary artery disease (CAD). Angina results from an imbalance between the heart’s oxygen demand and supply due to restricted blood flow in the coronary arteries. Nicorandil offers a dual mechanism of action — acting both as a nitrate-like vasodilator and a potassium channel opener, making it unique among anti-anginal agents.\n\nBy improving oxygen delivery to the myocardium and reducing cardiac workload, Nicorandil 5 mg Tablets provide effective relief from anginal pain and reduce the frequency and severity of ischemic episodes. It is also beneficial in preventing future attacks, improving exercise tolerance, and enhancing the overall quality of life in patients with chronic stable angina.\n\nComposition\n\nEach tablet contains:\n\nNicorandil IP – 5 mg\n\nExcipients – q.s.\n\nNicorandil tablets are available in film-coated form to ensure stability, easy swallowing, and optimal absorption. They are manufactured in compliance with Good Manufacturing Practices (GMP) standards to ensure safety, purity, and efficacy.\n\nPharmacological Action / Mechanism of Action\n\nNicorandil exhibits a dual mechanism that makes it distinct among anti-anginal drugs:\n\nNitrate-Like Effect:\nNicorandil acts as a nitric oxide (NO) donor. Nitric oxide activates guanylate cyclase, increasing cyclic GMP (cGMP) levels in vascular smooth muscle. This leads to relaxation of blood vessels, particularly veins and large arteries, thereby reducing preload and afterload on the heart. This nitrate-like activity lowers myocardial oxygen demand.\n\nPotassium Channel Opening Effect:\nNicorandil opens ATP-sensitive potassium (KATP) channels in vascular smooth muscle, resulting in arteriolar vasodilation. This increases coronary blood flow and improves oxygen supply to ischemic heart tissues.\n\nTogether, these effects reduce cardiac workload, enhance coronary perfusion, and prevent anginal pain by correcting the oxygen supply-demand mismatch in the heart muscle.\n\nUses and Indications\n\nNicorandil Tablets 5 mg are indicated for the treatment and prevention of angina pectoris in adults, particularly:\n\nChronic Stable Angina:\n\nHelps reduce the frequency and severity of chest pain associated with exertion or emotional stress.\n\nProphylaxis of Angina Attacks:\n\nUsed regularly to prevent anginal episodes, especially in patients with known coronary artery disease.\n\nAdjunct Therapy in Ischemic Heart Disease (IHD):\n\nCan be used alongside beta-blockers, calcium channel blockers, or antiplatelet drugs for enhanced symptom control and long-term protection.\n\nImprovement of Exercise Tolerance:\n\nReduces the likelihood of anginal pain during physical activity, enabling patients to perform daily tasks comfortably.\n\nIn some clinical cases, Nicorandil is also considered for post-myocardial infarction recovery, as it improves coronary perfusion, although this is at the discretion of a cardiologist.\n\nDosage and Administration\n\nRecommended Starting Dose: 5 mg to 10 mg twice daily.\n\nMaintenance Dose: May be increased gradually to 10–20 mg twice daily, depending on clinical response and tolerance.\n\nThe tablets should be swallowed whole with water, preferably at the same times each day.\n\nNicorandil should not be stopped abruptly; dosage tapering is recommended to avoid rebound angina.\n\nAlways follow the dosage instructions provided by the physician.\n\nKey Benefits\n\nDual Mechanism for Comprehensive Relief:\nCombines nitrate-like and potassium channel-opening properties for both arterial and venous dilation, providing superior protection against anginal attacks.\n\nImproves Coronary Blood Flow:\nDilates coronary arteries, increasing oxygen delivery to ischemic myocardial tissues.\n\nReduces Cardiac Workload:\nBy decreasing preload (venous return) and afterload (arterial resistance), Nicorandil minimizes the heart’s oxygen consumption.\n\nRapid Onset of Action:\nNicorandil acts within a short duration, offering quick relief from anginal discomfort.\n\nPrevents Future Angina Episodes:\nRegular use helps maintain steady control of chest pain, improving exercise capacity and quality of life.\n\nCompatible with Other Cardiac Medications:\nCan be safely used alongside antiplatelet agents, beta-blockers, ACE inhibitors, and statins as part of comprehensive cardiac care.\n\nFavorable Safety Profile:\nCompared to nitrates, Nicorandil carries a lower risk of tolerance development, making it suitable for long-term therapy.\n\nEnhances Myocardial Protection:\nNicorandil’s KATP channel activation provides additional cardioprotective effects by improving microvascular blood flow and limiting ischemic damage during stress.\n\nPrecautions and Warnings\n\nAlthough Nicorandil is generally well-tolerated, certain precautions are advised:\n\nHypotension:\nNicorandil may cause a drop in blood pressure due to vasodilation. Caution is advised in patients with hypotension or dehydration.\n\nConcurrent Use with Nitrates:\nShould not be used together with other nitrate medications to avoid severe hypotension.\n\nOral or Gastrointestinal Ulcers:\nRarely, Nicorandil may cause ulcerations in the mouth, intestines, or skin. Treatment should be discontinued if ulceration occurs.\n\nPatients with Low Blood Volume:\nUse cautiously in individuals with hypovolemia or those on diuretics.\n\nDriving and Machinery:\nDizziness or light-headedness may occur; avoid driving until effects are known.\n\nPregnancy and Lactation:\nShould be used only if prescribed by a physician when the potential benefits outweigh the risks.\n\nPossible Side Effects\n\nNicorandil is generally safe but may cause some side effects, particularly at the start of therapy or with higher doses. Common and rare adverse reactions include:\n\nCommon Side Effects:\n\nHeadache (due to vasodilation)\n\nFlushing or warmth sensation\n\nDizziness or light-headedness\n\nNausea or mild stomach upset\n\nFatigue or weakness\n\nLess Common / Rare Side Effects:\n\nHypotension (low blood pressure)\n\nPalpitations or tachycardia\n\nMouth ulcers, anal ulcers, or skin ulceration (uncommon but serious — discontinue if occurs)\n\nRash or allergic reaction\n\nVisual disturbances (rare and usually reversible)\n\nIf any severe reaction or persistent discomfort occurs, medical attention should be sought promptly.\n\nDrug Interactions\n\nAvoid concomitant use with nitrates or phosphodiesterase type-5 inhibitors (e.g., Sildenafil, Tadalafil), as it may cause a dangerous fall in blood pressure.\n\nCaution with antihypertensive drugs or diuretics, which may enhance hypotensive effects.\n\nAlcohol consumption can potentiate dizziness or hypotension and should be limited.\n\nStorage and Handling\n\nStore below 30°C, protected from moisture and direct sunlight.\n\nKeep out of reach of children.\n\nDo not use tablets past the expiry date or if the packaging is damaged.\n\nConclusion\n\nNicorandil Tablets 5 mg offer a modern and effective approach to managing angina pectoris, providing reliable relief through their dual-action mechanism. By combining nitrate-like vasodilation with potassium channel opening, Nicorandil ensures both oxygen supply improvement and reduction of cardiac workload — the cornerstone of angina management.\n\nIt is well-tolerated, fast-acting, and suitable for long-term therapy, making it a preferred choice for patients with chronic stable angina. Regular use under medical supervision helps reduce the frequency of chest pain, improve physical endurance, and enhance the overall quality of life in individuals with coronary artery disease.",
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