Desoximetasone Cream
Product Images NDC 68180-950

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 Desoximetasone (NDC 68180-950). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

Structure (D3270233 F3cd 4ea5 8f1c 0dcc16dd6dcb 01)

Structure (D3270233 F3cd 4ea5 8f1c 0dcc16dd6dcb 01)
Chemical structure diagram of desoximetasone, illustrating the arrangement of atoms and bonds specific to this corticosteroid active ingredient.*
FDA Label Image

Tube (D3270233 F3cd 4ea5 8f1c 0dcc16dd6dcb 02)

Tube (D3270233 F3cd 4ea5 8f1c 0dcc16dd6dcb 02)
Label for Desoximetasone Cream USP 0.25%, a topical human prescription drug by Lupin Pharmaceuticals. The label states the active ingredient concentration as 0.25%, net weight 15 g, and includes usage instructions and storage information. The label features dual barcodes, manufacturing details for Lupin Pharmaceuticals, Inc., and Lupin Limited India, and emphasizes topical use only.*
FDA Label Image

Carton (D3270233 F3cd 4ea5 8f1c 0dcc16dd6dcb 03)

Carton (D3270233 F3cd 4ea5 8f1c 0dcc16dd6dcb 03)
Packaging label for Desoximetasone Cream USP 0.25%, a topical human prescription drug by Lupin Pharmaceuticals, Inc. The label shows a 15 g tube containing 0.25% strength cream. It includes usage restrictions, manufacturer information, and instructions for puncturing the tube seal. The design features yellow and green highlights with 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.