Bexarotene Gel
Product Images NDC 69238-2088
View Photos of 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.
Product Images & Figures Index
Carton (Bexarotene Gel 1 Percent 2)
This is a medication information label for a gel containing 10 mg of bexarotene per gram. The gel also contains dehydrated alcohol, polyethylene glycol 400, hydroxypropyl cellulose, and butylated hydroxytoluene. There are instructions on how to open the tube and the pharmacist is advised to provide the enclosed prescribing information to the patient. The usual dosage and storage instructions are also provided. The medication is for topical use only and not for ophthalmic use. This medication is distributed by Amneal Pharmaceuticals LLC located in Bridgewater, NJ.*
Tube (Bexarotene Gel 1 Percent 3)
Bexarotene Gel, 1% is a prescription medication used for topical use only and should not be used for ophthalmic purposes. Each 60-gram tube contains 10mg of bexarotene along with other ingredients. The usual dosage should be followed as per the prescribing information. The tube has the Lot Number and Expiration Date printed on the crimp end, and it should be stored between 20°C to 25°C. Amneal Pharmaceuticals LLC distributes this gel.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.