Desonide Gel
Product Images NDC 24470-920

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Desonide (NDC 24470-920). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cintex Services, 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

Carton.jpg (Carton)

Desonide Gel, 0.05% is a topical medication for skin application only. It is available in 60g packing, with NDC code 20470-520-60. The active ingredient is Desonide 0.05%, and it should be applied to the affected area twice daily. The gel contains carbopol, edetate, tylose, sodium benzoate, methylparaben, propylene glycol, purified water, and sodium hydroxide. The medication is not for oral, ophthalmic, or intravaginal use. The packaging contains a warning to keep it out of reach of children and it is only for external use.*

FDA Label Image

Structure (Structure)

* 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.