Metronidazole Cream
Product Images NDC 59651-770

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metronidazole (NDC 59651-770). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Package Label-principal Display Panel (45 g Tube Label)

Package Label-principal Display Panel (45 g Tube Label)
Label for Metronidazole Topical Cream 0.75% (7.5 mg/g) in a 45 g tube. The label indicates it is for topical use only, not ophthalmic use. It is labeled as prescription only and distributed by Aurobindo Pharma USA, Inc. The label includes active and inactive ingredient details, storage instructions, and a barcode. Manufactured in India.*
FDA Label Image

Package Label-principal Display Panel (45 g Tube Carton)

Package Label-principal Display Panel (45 g Tube Carton)
Metronidazole Topical Cream 0.75% packaging label for a 45 g tube. The label states it is for topical use only, not for ophthalmic use, and is Rx only. It lists the active ingredient strength as metronidazole USP 0.75% (7.5 mg/g) and includes storage instructions. The product is distributed by Aurobindo Pharma USA, Inc., made in India. Barcode and various regulatory and batch printing details are visible.*
FDA Label Image

Str (Metronidazole Str)

Str (Metronidazole Str)
Chemical structure of metronidazole, showing a nitroimidazole core with a nitro group (O2N), methyl group (CH3), and a hydroxyl-ethyl side chain (CH2CH2OH) attached to the imidazole ring.*

* 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.