Image (E52543e3 9fd5 4a91 A9cb Ce5eec8116d1 01)
Metronidazole Gel
Product Images NDC 62332-630
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metronidazole (NDC 62332-630). 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.
45 G Carton Label (E52543e3 9fd5 4a91 A9cb Ce5eec8116d1 02)
Metronidazole Gel USP, 1% is a prescription-only medication that comes in 45-gram tubes for topical use only. This medication should not be used orally, ophthalmically, or intravaginally. Metronidazole Gel USP, 1% contains 10 mg (1%) metronidazole USP as an active ingredient, and the gel base consists of etadex, edetate disodium, hydroxyethyl cellulose, methyparaben, nicotinamide, phenoxyethanol, propylene glycol, propylparaben, and purified water. The usual dosage is applying the gel once per day to the affected area. Instructions for use are included in the prescribing information. This medication should be stored at a temperature range of 20°C to 25°C (66°F to 77°F), with excursions permitted between 15°C to 30°C (59°F to 86°F). Keep out of reach of children. Alembic Pharmaceuticals, Inc. manufactures Metronidazole Gel USP, 1% for Aleor Dermaceuticals Ltd.*
55 G Pump Carton Label (E52543e3 9fd5 4a91 A9cb Ce5eec8116d1 03)
This is description of a medication called Metronidazole Gel USP 1%. It's a topical gel that contains metronidazole USP as the active ingredient. The gel is not for oral, ophthalmic or intravaginal use. It should be applied to the affected area(s) only as per instructions provided in the prescribing information. It is stored at temperatures between 15°C to 30°C, which is between 59°F to 86°F. The prescription is only for the use of the person named, and should be kept out of reach of children. The NDC code, which is a unique identifier for this medicine, is 62332-630-55.*
* 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.
