Tretinoin Gel
Product Images NDC 59651-712

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tretinoin (NDC 59651-712). 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

Figure (Tretinoin Fig1)

An instructional illustration showing a person applying topical gel to three facial areas: the forehead, nose, and chin using a finger. The image is intended to demonstrate application sites for the topical medication gel.*

FDA Label Image

Package Label.principal Display Panel- 15 G Tube Label (Tretinoin Fig2)

Label for Tretinoin Gel USP 0.01% topical gel, net weight 15 g, manufactured by Aurobindo Pharma Limited. The label includes dosage strength, usage warning to keep out of reach of children, storage instructions, and distributor information (Aurobindo Pharma USA, Inc., East Windsor, NJ). Contains active ingredient tretinoin 0.1 mg per gram.*

FDA Label Image

Package Label.principal Display Panel- 15 G Tube Carton (Tretinoin Fig3)

Packaging label for Tretinoin Gel, USP 0.01% topical gel in a 15 g tube. Label shows the drug is for topical use only, includes warnings to keep out of reach of children, and storage instructions. Labeler is Aurobindo Pharma Limited, with distribution by Aurobindo Pharma USA, Inc. The NDC number 59651-712-14 is visible. Additional information includes instructions for opening and ingredients like alcohol and excipients.*

FDA Label Image

Str (Tretinoin Str)

Chemical structure of tretinoin showing its molecular formula with carbon, hydrogen, and carboxyl groups in a polyene chain and cyclohexene ring arrangement.*

* 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.