Tretinoin Cream
Product Images NDC 51672-1395

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tretinoin (NDC 51672-1395). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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.

FDA Label Image

Chemical Structure (Tretinoin 01)

Chemical structure of tretinoin, showing its characteristic polyene chain with conjugated double bonds and carboxyl group, consistent with the active ingredient in Tretinoin cream 1 mg/g.*

FDA Label Image

Figure (Tretinoin 02)

An instructional black-and-white illustration showing a woman applying cream to multiple marked spots on her face using her fingers, demonstrating the topical application process.*

FDA Label Image

Principal Display Panel (20 g Tube Carton)

Packaging label for Tretinoin Cream USP, 0.1%, 20 g tube, for topical use only. The label shows the brand name Tretinoin with strength 0.1% cream, and includes directions to keep out of reach of children. The product is labeled Rx only and manufactured by Sun Pharmaceutical Industries, Inc., with distribution by Taro Pharmaceuticals U.S.A., Inc. The packaging includes storage instructions and a barcode.*

* 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.