Urea 40 Percent Cream
Product Images NDC 58657-487

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Urea 40 Percent (NDC 58657-487). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Method Pharmaceuticals, 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

Urea Is A Diamide Of Carbonic Acid With The Following Chemical Structure: (Urea 41 Percent Cream 01)

Chemical structure of urea showing its molecular formula with two amine groups (NH2) bonded to a carbonyl group (C=O).*

FDA Label Image

Label (Urea1oz)

Label for Urea Cream 40%, topical cream containing 400 mg/g urea, manufactured by Method Pharmaceuticals, LLC. The label states prescription use only and provides storage instructions. The package size shown is 1 oz (28.35 g). The label includes a barcode and lists inactive ingredients such as carbomer, cetearyl alcohol, glycerin, and mineral oil.*

FDA Label Image

Label (Urea3oz)

Label for Urea Cream 40% topical cream by Method Pharmaceuticals, LLC. The label includes the product name, strength (40%), and indicates it is for topical use only, not for ophthalmic use. It lists inactive ingredients and storage instructions to keep at room temperature between 15°C-30°C, protect from freezing, and keep the bottle tightly closed. The package size is 3 oz (85 g).*

FDA Label Image

Label (Urea7oz)

Urea Cream 40% topical cream in a 7 oz (198.4 g) container, labeled for prescription use only. The label shows the product is for topical use and not for ophthalmic use. It is manufactured by Method Pharmaceuticals, LLC. Ingredients and storage instructions are printed on the label, along with the NDC 58657-487-07.*

* 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.