Tretinoin Cream
Product Images NDC 16714-250

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tretinoin (NDC 16714-250). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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 diagram of Tretinoin, showing its molecular composition with multiple double bonds, methyl groups, and a carboxyl group. The structure is consistent with the active ingredient in the topical cream labeled Tretinoin 1 mg/g by NORTHSTAR RX LLC.*

FDA Label Image

Image (Tretinoin 02)

An instructional illustration showing a woman applying topical cream to her face. The diagram highlights several spots on her face where the cream is to be applied, indicating method of use for topical medication like Tretinoin cream.*

FDA Label Image

Principal Display Panel (20 g Tube Carton)

Packaging label for Tretinoin Cream USP 0.1% topical cream, 20 g tube. The label features the NorthStar Rx LLC brand, with NDC 16714-250-01. Manufacturing information includes Taro Pharmaceuticals Inc. and Northstar Rx LLC. The label notes the cream is for topical use only and is prescription only (Rx).*

* 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.