Betamethasone Dipropionate Cream, Augmented
Product Images NDC 51672-1310

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Betamethasone Dipropionate (NDC 51672-1310). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure (Betamethasone 01)

Chemical structure of betamethasone dipropionate, a corticosteroid active ingredient, showing its molecular arrangement with functional groups including ketones, hydroxyl groups, and ester moieties.*

FDA Label Image

Principal Display Panel (15 g Tube Carton)

Betamethasone Dipropionate Cream USP (Augmented), 0.05%, 15 g tube packaging label. The label states it is for dermatologic use only, not for ophthalmic use, and is Rx only. The product is manufactured by Taro Pharmaceuticals and distributed by Taro Pharmaceuticals U.S.A., Inc. Warnings include keeping out of reach of children and storage instructions. Strength is expressed as betamethasone.*

* 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.