Bexarotene Gel
Product Images NDC 69238-2088

3 FDA label images from Amneal Pharmaceuticals Ny Llc · 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 Bexarotene (NDC 69238-2088). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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

Structural Formula (Bexarotene Gel 1 Percent 1)

Structural Formula (Bexarotene Gel 1 Percent 1)
Chemical structure of the active ingredient Bexarotene, showing its molecular formula with carbon, hydrogen atoms and a carboxylic acid group, consistent with its topical gel formulation by Amneal Pharmaceuticals.*
FDA Label Image

Carton (Bexarotene Gel 1 Percent 2)

Carton (Bexarotene Gel 1 Percent 2)
Packaging label for Bexarotene Gel 1%, containing 10 mg of bexarotene per gram. The topical gel product is distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. The label states it is for topical use only and not for ophthalmic use, with a net weight of 60 grams. Instructions and warnings about product storage and use are included, along with the product NDC 69238-2088-6 and barcode.*
FDA Label Image

Tube (Bexarotene Gel 1 Percent 3)

Tube (Bexarotene Gel 1 Percent 3)
Label for Bexarotene Gel, 1% topical gel by Amneal Pharmaceuticals LLC. The label states "Not For Ophthalmic Use" and "For Topical Use Only," with a net weight of 60 grams. It also includes usage instructions, storage conditions, active ingredient strength (10 mg/g), and a barcode. The NDC is 69238-2088-6.*

* 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.