Adapalene And Benzoyl Peroxide Gel
Product Images NDC 46708-662

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Adapalene And Benzoyl Peroxide (NDC 46708-662). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Limited, 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 (528fc681 2ba1 442f 812f 339f90b0a030 01)

Chemical structure diagram of adapalene, the active ingredient in adapalene and benzoyl peroxide topical gel by Alembic Pharmaceuticals Limited.*

FDA Label Image

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Chemical structure of a compound representing the active ingredient related to adapalene and benzoyl peroxide topical gel. The structure includes aromatic rings and ester functional groups, consistent with benzoyl peroxide's chemical features.*

FDA Label Image

Pump Label (528fc681 2ba1 442f 812f 339f90b0a030 03)

Label for Adapalene and Benzoyl Peroxide Topical Gel USP, 0.3%/2.5%, 45 grams, by Alembic Pharmaceuticals Limited. The label states Rx only, for topical use only, and includes storage instructions. Active ingredients adapalene 0.3% and benzoyl peroxide 2.5% per gram of gel are listed along with inactive ingredients. The label includes barcode and manufacturing details from Alembic Pharmaceuticals Limited, Karakhadi, Vadodara, India.*

FDA Label Image

Carton Label (528fc681 2ba1 442f 812f 339f90b0a030 04)

Packaging label for Adapalene and Benzoyl Peroxide Topical Gel USP, 0.3%/2.5%, a topical prescription gel. The label shows the product name, strength, and form, specifies use via pump dispensing, and indicates a 45-gram package. Manufacturer is Alembic Pharmaceuticals Limited. The label includes storage instructions, usage directions, and ingredient information, as well as NDC 46708-662-45.*

* 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.