NU-DERM SYSTEM NORMAL-DRY
NU-DERM SYSTEM NORMAL DRY Skin Transformation Kit
Approved
Approval ID
0d91be8e-1553-4ef7-b333-724c0e27651e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 15, 2013
Manufacturers
FDA
OMP, INC.
DUNS: 790553353
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Hydroquinone, Octinoxate, and Zinc Oxide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code62032-520
Product Classification
G
Generic Name
Hydroquinone, Octinoxate, and Zinc Oxide
Product Specifications
Effective DateAugust 15, 2013
FDA Product Classification