Topicort Spray
Product Images NDC 51672-5281

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Topicort (NDC 51672-5281). 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 (Topicort 01)

Chemical structure of desoximetasone, the active ingredient in Topicort 2.5 mg/mL topical spray by Sun Pharmaceutical Industries, Inc., showing its molecular configuration including hydroxyl, methyl, fluoro, and ketone groups.*

FDA Label Image

Figure A (Topicort 02)

An instructional diagram showing the parts of a spray bottle for Topicort (Desoximetasone) topical spray. Labeled components include the cap, pump top, opening, and bottle. The image visually explains the spray bottle design for the medication.*

FDA Label Image

Figure B (Topicort 03)

A photograph showing a hand holding and pressing the nozzle of a white topical spray bottle, demonstrating the act of spraying the medication.*

FDA Label Image

Figure C (Topicort 04)

An image showing a person administering a topical spray to their elbow. The photo illustrates the application of a spray medication on the skin, relevant to topical products like Topicort (desoximetasone) spray.*

FDA Label Image

Figure D (Topicort 05)

An instructional image showing hands holding a white topical spray bottle, demonstrating the act of placing or removing a clear protective cap on the spray nozzle. The background is plain, focusing on the spray bottle usage.*

FDA Label Image

Principal Display Panel (100 mL Bottle Carton)

Packaging label for Topicort 0.25% (desoximetasone) Topical Spray, 100 mL, a prescription topical medication. The label features dosage strength, product form, usage instructions, inactive ingredients, and storage warnings. It is manufactured by Taro Pharmaceuticals Inc. and distributed by TaroPharma, with NDC 51672-5281. The design includes dosage and pharmacist instructions, and a barcode.*

* 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.