Desoximetasone Cream
Product Images NDC 51672-1271

4 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Desoximetasone (NDC 51672-1271). 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 (Desoximetasone 01)

Chemical Structure (Desoximetasone 01)
Chemical structure diagram of desoximetasone, showing the arrangement of carbon, hydrogen, oxygen, and fluorine atoms in the molecule.*
FDA Label Image

Principal Display Panel (0.05%, 15 g Cream Carton)

Principal Display Panel (0.05%, 15 g Cream Carton)
Packaging label for Desoximetasone Cream USP 0.05%, topical cream in a 15 g tube. The label includes dosage form and strength, instructions for use, storage conditions, manufacturer information (Taro Pharmaceuticals Inc.), and cautionary statements about use and keeping out of reach of children. The label also features barcodes and the NDC 51672-1271-1.*
FDA Label Image

Principal Display Panel (0.25%, 15 g Cream Carton)

Principal Display Panel (0.25%, 15 g Cream Carton)
Desoximetasone Cream USP 0.25% topical cream packaging label by Taro Pharmaceuticals. The label indicates a 15 g tube, with instructions for topical use only and warnings to keep out of reach of children. The label includes manufacturer and distributor information, a barcode, and storage instructions.*
FDA Label Image

Principal Display Panel (0.05%, 15 g Gel Carton)

Principal Display Panel (0.05%, 15 g Gel Carton)
Packaging label for Desoximetasone Gel USP 0.05%, 15 g tube by Taro Pharmaceuticals. The label indicates topical use only, not for oral, ophthalmic, or intravaginal use. It includes product identification, NDC 51672-1261-1, storage instructions, directions for tube seal puncture, barcode, and a caution to keep medication out of reach of children. The label design features green, red, and black text on a white background.*

* 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.