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Adapalene Gel
Product Images NDC 62332-549
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Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Adapalene (NDC 62332-549). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Alembic Pharmaceuticals Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
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Adapalene Gel is a medication applied topically once a day at nighttime to affected areas for acne treatment. It contains Adapalene USP, 0.3% (3mg), carbopol 980, edetate disodium, methylparaben, poloxamer 124, propylene glycol, purified water, and sodium hydroxide. It is manufactured by Aleor Dermaceuticals Ltd. For complete prescribing information, see the package insert. Keep it out of the reach of children, and store at 68° to 77°F (20° to 25°C). The lot number and expiry date are printed/embossed below the crimp. This medicine is for external use only and not for ophthalmic, oral, or intravaginal use.*
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This is a product description for a Baich Coding and Barcode product with LOT and serial numbers, and a SAP code. It also mentions a medication called Adapalene Gel USP, which is for external use only and should not be used orally or intravaginally. The medication is contained in a 45g container and contains carbopol 980, edetate disodium, methylparaben, poloxamer 124, propylene glycol, purified water, and sodium hydroxide in an aqueous gel. It also contains a warning to keep all medications out of the reach of children and the recommended dosage of application, which should be done once a day at bedtime to affected areas. The product should be stored at controlled room temperature and protect it from freezing. The product is manufactured by Alembic Pharmaceuticals Inc.*
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This is a description of Adapalene Gel USP, a medication for external use only that contains 0.3% Adapalene USP. The medication is used to treat affected areas by applying a thin film at nighttime. The gel consists of water, carbopol, edetate disodium, methylparaben, poloxamer 124, propylene glycol, purified water, sodium hydroxide, and may contain hydrochloric acid for pH adjustment. It is manufactured by Aleor Dermaceuticals L. and Alembic Pharmaceuticals, Inc. It is essential to store the medication at a controlled room temperature and keep it out of reach of children. The lot number and expiry date can be found on the crimp of the tube. SAP Code is not available.*
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This is a description of Adapalene Gel USP. It contains 0.3% Adapalene USP and is meant for external use only. The usual dosage is a thin film applied once daily to affected areas. It should be kept away from children and should not be used orally, intravaginally, or in the eyes. It is manufactured by Alembic Pharmaceuticals and Aleor Dermaceuticals Ltd. and should be stored at a controlled room temperature. The text also includes information about the ingredients and the lot and expiry date.*
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NDC 62332-549-15 is a prescription medication called Adapalene Gel USP. It should only be used externally and not for oral, intravaginal, or ophthalmic purposes. Each gram of the medication contains Adapalene USP 0.3% (3 mg) in an aqueous gel. It is recommended to apply a thin film once a day at night to affected areas. The gel consists of carbopol 980, edetate disodium, methylparaben, poloxamer 124, propylene glycol, purified water, and sodium hydroxide. The manufacturing is done by Alembic and is stored at controlled room temperature. It is crucial to keep this medication away from the reach of children.*
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This is a description of Adapalene Gel USP, used for external application, with a net weight of 15 g. It is manufactured by Aleor Dermaceuticals Ltd. and contains 0.3% Adapalene USP in an aqueous gel formulation consisting of carbopol 980, edetate disodium, methylparaben, poloxamer 124, propylene glycol, purified water, and sodium hydroxide. Hydrochloric acid may be used for pH adjustment. It should be applied once a day at nighttime to affected areas. Storage should be at a controlled room temperature between 68° to 77°F (20° to 25°C) with excursions between 59°to 86°F (15°to 30°C) permitted. Lot number, expiration date, and barcode details are also provided.*
* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
