Desoximetasone Spray
Product Images NDC 51672-1396

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Desoximetasone (NDC 51672-1396). 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 of desoximetasone, showing its steroidal framework with hydroxyl, keto, fluorine, methyl, and aldehyde functional groups clearly depicted in a line-angle representation.*

FDA Label Image

Figure A (Desoximetasone 02)

An instructional illustration labeling parts of a topical spray bottle for Desoximetasone 2.5 mg/mL. The diagram identifies the cap, pump top, opening, and bottle to show the spray packaging components.*

FDA Label Image

Figure B (Desoximetasone 03)

Desoximetasone 2.5 mg/mL topical spray in a white plastic bottle with a spray pump, held in a person's hand. The label or additional markings are not visible.*

FDA Label Image

Figure C (Desoximetasone 04)

A photograph showing a person applying Desoximetasone topical spray to the skin near the elbow. The image illustrates the use of a white spray bottle with a nozzle to deliver the medication topically to the affected area.*

FDA Label Image

Figure D (Desoximetasone 05)

An instructional image showing hands demonstrating how to use a topical spray bottle, with one hand holding the white spray bottle and the other hand positioned to press the spray nozzle.*

FDA Label Image

Principal Display Panel (100 mL Bottle Carton)

Desoximetasone 0.25% Topical Spray packaging label displays a 100 mL bottle size. The label highlights it is for topical use only and not for oral, ophthalmic, or intravaginal use. It includes instructions for pharmacists, ingredient details, storage information, and flammability warnings. The labeler is identified as Sun Pharmaceutical Industries, Inc., with distribution by Taro Pharmaceuticals U.S.A., Inc.*

* 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.