MedPath

UREA

UREA CREAM 39%

Approved
Approval ID

0fa3f9de-9183-b6b9-e063-6394a90aadb4

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 23, 2024

Manufacturers
FDA

Cintex Services, LLC

DUNS: 078304114

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

UREA

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code24470-938
Product Classification
G
Generic Name
UREA
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 23, 2024
FDA Product Classification

INGREDIENTS (1)

UREAActive
Quantity: 390 mg in 1 g
Code: 8W8T17847W
Classification: ACTIB

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