Tretinoin Cream
Product Images NDC 72578-155

3 FDA label images from Viona Pharmaceuticals Inc · 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 Tretinoin (NDC 72578-155). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viona Pharmaceuticals 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

Image (22150db5 D543 419f Bc09 A3280e19777b 01)

Image (22150db5 D543 419f Bc09 A3280e19777b 01)
Chemical structure diagram of tretinoin, showing its molecular arrangement with multiple methyl groups attached to a bicyclic ring system and a carboxylic acid functional group.*
FDA Label Image

Image (22150db5 D543 419f Bc09 A3280e19777b 02)

Image (22150db5 D543 419f Bc09 A3280e19777b 02)
An instructional illustration of a woman's face showing application points for topical treatment, with dots marked on the forehead, cheeks, and chin. The woman is applying cream with two fingers on one cheek.*
FDA Label Image

Tube Label (22150db5 D543 419f Bc09 A3280e19777b 03)

Tube Label (22150db5 D543 419f Bc09 A3280e19777b 03)
Tretinoin Cream USP 0.025% topical cream label from Viona Pharmaceuticals Inc. The 20 g prescription drug label includes instructions for use, storage conditions (20 to 25°C), warnings about seal integrity, and manufacturer information (Zydus Lifesciences Ltd, India). The label states the active ingredient concentration as 0.025% and notes it is Rx only.*

* 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.