Desoximetasone Cream
Product Images NDC 68180-949

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 68180-949). 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.

Product Images & Figures Index

FDA Label Image

Structure (3c01bc6e 9551 41df 9500 644a6d58aba8 01)

Structure (3c01bc6e 9551 41df 9500 644a6d58aba8 01)
Chemical structure diagram of desoximetasone, showing its steroid backbone with hydroxyl, fluorine, methyl, and aldehyde functional groups as labeled in the molecular structure.*
FDA Label Image

Tube (3c01bc6e 9551 41df 9500 644a6d58aba8 02)

Tube (3c01bc6e 9551 41df 9500 644a6d58aba8 02)
Desoximetasone Cream USP 0.05% topical cream label from Lupin Pharmaceuticals, Inc. The label includes usage instructions, storage conditions, and manufacturer information. It specifies the product is for topical use only, not for oral, ophthalmic, or intravaginal use, contains 15 g per tube, and includes two barcodes and an NDC number 68180-949-01.*
FDA Label Image

Carton (3c01bc6e 9551 41df 9500 644a6d58aba8 03)

Carton (3c01bc6e 9551 41df 9500 644a6d58aba8 03)
Packaging label for Desoximetasone Cream USP 0.05%, a topical prescription drug. The label shows the product name, strength, and dosage form prominently with the NDC 68180-949-01. It also includes directions, storage information, and manufacturer details for Lupin Pharmaceuticals, Inc. The tube contains 15 grams of cream.*

* 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.