Desoximetasone Ointment
Product Images NDC 72578-095

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Desoximetasone (NDC 72578-095). 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

Structured Product Formula For Desoximetasone (9e0563ea D785 4735 Bd69 3c5eefa842ab 01)

Chemical structure of desoximetasone, showing its steroid backbone with fluorine and hydroxyl functional groups highlighted. The diagram displays atom connectivity and bonds typical of this corticosteroid molecule.*

FDA Label Image

Desoximetasone Oinment, 0.25 (9e0563ea D785 4735 Bd69 3c5eefa842ab 02)

Label for Desoximetasone Ointment, USP 0.25% strength in a 15 g tube. The ointment contains 2.5 mg desoximetasone per gram. Label includes usage instructions, storage conditions, and manufacturing and distribution information by Viona Pharmaceuticals Inc. and Cadila Healthcare Ltd. The label features the NDC 72578-095-01 and highlights that the product is for topical external use only.*

FDA Label Image

Carton Label (9e0563ea D785 4735 Bd69 3c5eefa842ab 03)

Packaging label for Desoximetasone Ointment USP 0.25%, topical ointment in a 15 g tube. The label includes usage warnings restricting use to external application only and advises keeping out of reach of children. The product is labeled as prescription only and is distributed by Viona Pharmaceuticals Inc. Additional information on storage conditions, dosage, and puncturing instructions for the tube seal are also present.*

* 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.