Urea Cream
Product Images NDC 24470-939

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Urea (NDC 24470-939). 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 (Carton1)

Packaging label for Urea Cream 40%, topical cream in a 1 oz (28.35 g) tube. The label includes the proprietary name Urea Cream with the strength indicated as 40%. The labeler is Cintex Services, LLC, located in Dallas, TX. The label contains usage instructions, dosage guidelines, storage information, precautions, and a barcode. The container is marked Rx Only and includes a serial number label area.*

FDA Label Image

Label3 (Label3)

Text label of Urea Cream 40%, topical prescription drug containing 400 mg urea per gram. The label includes description, indications for use in hyperkeratotic skin conditions, dosage and administration instructions, warnings, precautions, storage guidelines, manufacturer information (Cintex Services, LLC), and a barcode with NDC 24470-939. The net weight is 3 oz (85 g).*

FDA Label Image

Label7 (Label7)

Label for Urea Cream 40%, topical cream containing 400 mg/g of urea. The label includes product details such as net weight of 7 oz (198.4 g), usage directions, warnings, storage instructions, and manufacturer Cintex Services, LLC of Dallas, TX. It also displays an NDC barcode and notes it is Rx only.*

FDA Label Image

Structure (Structure)

Chemical structure of UREA, showing its molecular formula with two amine groups attached to a carbonyl group.*

* 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.