Desonide Cream
Product Images NDC 0713-0661

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Desonide (NDC 0713-0661). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosette 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

Structure (Structure1)

Chemical structure of desonide, showing its steroidal framework with hydroxyl and ketone functional groups, along with ester linkages consistent with its molecular composition.*

FDA Label Image

Carton 15 (Carton 15g)

The packaging label for Desonide Cream 0.05%, a topical prescription drug by Cosette Pharmaceuticals, Inc. The label shows a 15 g tube size, with instructions noting external use only and not for ophthalmic use. It includes storage instructions, puncture seal directions, and a barcode with NDC 0713-0661-15. Ingredients and usual dosage information are listed on the package.*

FDA Label Image

Carton 60 (Carton 60g)

Desonide Cream 0.05% topical cream packaging label for a 60 g tube, labeled Rx only. The label includes usage warnings, storage instructions, a barcode, and lists Cosette Pharmaceuticals, Inc. as the manufacturer. The strength is prominently displayed as 0.05%, and the NDC number 0713-0661-60 is visible.*

FDA Label Image

Tube 15 (Tube 15g)

Desonide Cream 0.05% topical cream label showing a 15 g tube by Cosette Pharmaceuticals, Inc. The label displays the NDC 0713-0661-15 with usage instructions, storage conditions, ingredients, and a barcode, emphasizing it is for external use only and prescription-only.*

FDA Label Image

Tube 60 (Tube 60g)

Desonide Cream 0.05% topical cream in a 60 g container. The label states it is for external use only and is Rx only. Manufactured by Cosette Pharmaceuticals, Inc., South Plainfield, NJ. The label includes usage instructions, ingredient details, storage temperature, and a barcode with NDC 0713-0661-60.*

* 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.