Tretinoin Cream
Product Images NDC 62032-414

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Tretinoin Cream (NDC 62032-414). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Obagi Cosmeceuticals 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

219c9161 E2cc 479d 820a 12e62e5a93ca 00

An instructional illustration showing a female face with dot markings on the forehead, cheeks, nose, and chin. A hand with two fingers is positioned near the left cheek, indicating application of a topical cream to the facial spots.*

FDA Label Image

Chemicalstructure.jpg (Image 01)

Chemical structure diagram of tretinoin, the active ingredient in Tretinoin Cream by Obagi Cosmeceuticals LLC. The image shows the molecular structure with multiple double bonds and methyl groups, plus a carboxylic acid group at one end.*

FDA Label Image

Image 03

Packaging label for Tretinoin Cream USP 0.1% by Obagi Cosmeceuticals LLC. The 0.7 oz (20 g) topical cream box includes dosage instructions, warning, and storage information. The label displays the NDC 62032-417-20, barcode, ingredient list including tretinoin 0.1%, and manufacturer details. The design uses beige, black, and white colors with the Obagi Medical logo.*

FDA Label Image

Image 04

Packaging label for Tretinoin Cream USP 0.05%, topical cream in a 0.7 oz (20 g) tube. The label displays the Obagi Medical logo and indicates prescription use only. It includes warnings, usage instructions, ingredient list, barcode, and distributor information for Obagi Cosmeceuticals LLC. The design features a predominantly white background with a teal accent panel.*

FDA Label Image

Image 05

Packaging label for Tretinoin Cream USP 0.025% topical cream, 0.7 oz (20 g) tube, by Obagi Cosmeceuticals LLC. The label includes dosage instructions, a warning to keep out of reach of children, and a list of ingredients. The label displays the NDC 62032-414-20, manufacturer information, and the product is marked 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.