Desoximetasone Cream
Product Images NDC 72578-091

3 FDA label images from Viona Pharmaceuticals Inc · 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 72578-091). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viona 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

Desoximetasone Cream Usp, 0.25% (A0cff08d 36d5 4b77 8647 F4b33ed4f9b5 01)

Desoximetasone Cream Usp, 0.25% (A0cff08d 36d5 4b77 8647 F4b33ed4f9b5 01)
Chemical structure diagram of desoximetasone, showing its steroid backbone with labeled functional groups including hydroxyl, keto, and fluorine substituents.*
FDA Label Image

Desoximetasone Cream Usp, 0.25% (A0cff08d 36d5 4b77 8647 F4b33ed4f9b5 02)

Desoximetasone Cream Usp, 0.25% (A0cff08d 36d5 4b77 8647 F4b33ed4f9b5 02)
Label for Desoximetasone Cream, USP 0.25% topical cream in a 15 g tube. The label states the active ingredient strength as 2.5 mg/g and includes usage instructions, storage conditions, and manufacturer information (Cadila Healthcare Ltd, India) as well as the distributor (Viona Pharmaceuticals Inc, Cranford, NJ). The label also includes the product NDC 72578-091-01 and a barcode.*
FDA Label Image

Desoximetasone Cream Usp, 0.25% (A0cff08d 36d5 4b77 8647 F4b33ed4f9b5 03)

Desoximetasone Cream Usp, 0.25% (A0cff08d 36d5 4b77 8647 F4b33ed4f9b5 03)
The packaging label for Desoximetasone Cream, USP 0.25% strength, topical cream in a 15 g package. It states it is for topical use only, not for oral, ophthalmic, or intravaginal use. The label includes manufacturer information (Cadila Healthcare Ltd, India) and distributor details (Viona Pharmaceuticals Inc, Cranford, NJ). The label also has dosing instructions and storage information, barcode, and NDC number 72578-091-01.*

* 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.