Urea 39 Cream
Product Images NDC 87021-602

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Urea 39 (NDC 87021-602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Krewe Pharma, 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.

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FDA Label Image

Urea 39 (Urea 39 Label)

Urea 39 (Urea 39 Label)
This is a description of a skincare product containing 39% urea, intended for intensely exfoliating and softening very dry, rough, and thickened skin. It can be applied twice a day or as directed by a physician. The cream helps improve the appearance of rough patches, calluses, and thickened nails. It is important to avoid contact with eyes, lips, or mucous membranes while using the product. Discontinue use if irritation occurs and keep out of reach of children. The product is dispensed by prescription and manufactured in the USA. For storage, it should be kept at 20° to 25°C (68°F to 77°F), protected from freezing and excessive heat. For further information, contact the manufacturer Krewe Pharma at their specified address and phone number or visit their website.*

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