Desonide Cream
Product Images NDC 16714-729

View Photos of Packaging, Regulatory Labels, and Product Appearance

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)

FDA Label Image

Principal Display Panel (60 g Tube Carton)

Principal Display Panel (60 g Tube Carton)
Desonide Cream is a topical medication that contains 0.5 mg of desonide in a cream base of aluminum acetate basic. The cream also includes cetearyl alcohol, sodium lauryl sulfate/sodium cetzant sulfate, glycerin, mineral oil, purified water, white petrolatum, and white wax. It should be applied two to four times a day to the affected area. This medication is not intended for ophthalmic use and should be stored at a temperature of 20°C to 25°C (68°F to 77°F). The manufacturer is Northstar Rx LLC, with production by Taro Pharmaceuticals Industries Ltd. For full prescribing information, refer to the package insert.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.