Desonide Cream
Product Images NDC 16714-729

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Desonide (NDC 16714-729). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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 (Desonide 01)

Chemical structure diagram of Desonide, showing its steroid backbone with associated functional groups as typically represented in pharmaceutical labeling.*

FDA Label Image

Principal Display Panel (60 g Tube Carton)

Packaging label for Desonide Cream 0.05%, topical cream in a 60 g tube. The label includes usage instructions, storage conditions, and warnings for external use only, not for ophthalmic use. It shows the labeler as NorthStar Rx LLC and manufacturer as Taro Pharmaceutical Industries Ltd. The NDC number 16714-729-02 is displayed.*

* 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.