Urea Cream
Product Images NDC 44523-617

5 FDA label images from Biocomp Pharma, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Urea (NDC 44523-617). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Biocomp Pharma, Inc., 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

Carton1.jpg (Carton1)

Carton1.jpg (Carton1)
The label for UREA 40% Cream, topical medication by BioComp Pharma, Inc. It includes the active ingredient urea at 400 mg/g, presented in a 1 oz (28.35 g) cream tube. The label highlights Rx only status, storage instructions, and manufacturer information, along with a barcode and serialization label. The design uses teal and grey color blocks for the product name and strength.*
FDA Label Image

Label1.jpg (Label1)

Label1.jpg (Label1)
UREA 40% Cream topical formulation in a 1 oz (28.35 g) container. The label shows key ingredients, directions for use, storage conditions, manufacturer BioComp Pharma, Inc., and a barcode. It states the product is for external use only and not for ophthalmic use, with a detailed administration guide and safety warnings.*
FDA Label Image

Label2.jpg (Label2)

Label2.jpg (Label2)
Urea 40% Cream topical medication label by BioComp Pharma, Inc. The label shows the active ingredient urea at 400 mg/g strength in a cream dosage form. The net weight is 3 oz. (85 g). It includes usage instructions, warnings, storage conditions, and contact information for reporting adverse events. The label also displays the NDC code 44523-617-03 and the BioComp Pharma logo.*
FDA Label Image

Label3.jpg (Label3)

Label3.jpg (Label3)
Drug Facts panel for Urea 40% Cream, topical prescription drug by BioComp Pharma, Inc. It details a 400 mg/g urea concentration in the cream, lists ingredients, indications for treating hyperkeratotic skin and nail conditions, administration instructions, warnings, precautions, and storage guidelines. Includes contact info and barcode.*
FDA Label Image

Structure.jpg (Structure)

Structure.jpg (Structure)
Chemical structure of urea shown with a carbon atom double-bonded to an oxygen atom and single-bonded to two amine groups (NH2). This represents the molecular structure of the active ingredient urea used in the topical cream.*

* 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.