Metronidazole Gel
Product Images NDC 59651-813

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 59651-813). 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 (60 g Tube Label)

Package Label-principal Display Panel (60 g Tube Label)
Label of Metronidazole Gel USP 1% (10 mg/g) topical gel in a 60 g tube from Aurobindo Pharma Limited. The label shows the product name, concentration, and usage instructions limited to topical use. It includes storage details, ingredient list, distributor information, and a barcode. The label emphasizes Rx-only status and contains a section for batch details and expiration date.*
FDA Label Image

Package Label.principal Display Panel- 60 G Tube Carton (Metronidz Fig2)

Package Label.principal Display Panel- 60 G Tube Carton (Metronidz Fig2)
Packaging label for Metronidazole Gel USP 1% topical gel, net weight 60 grams. The label indicates for topical use only and Rx only. Labeler is Aurobindo Pharma Limited. The label also includes storage instructions, ingredients, and distributor information: Aurobindo Pharma USA, Inc., East Windsor, NJ. The product is made in India with NDC 59651-813-60.*
FDA Label Image

Chemical Structure (Metronidz Str)

Chemical Structure (Metronidz Str)
Chemical structure of metronidazole, displaying a nitroimidazole core with nitro, hydroxylethyl, and methyl functional groups attached to the 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.