NU-DERM SYSTEM NORMAL-DRY
NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION KIT
Approved
Approval ID
7e70faa2-ce6a-4815-9fa1-43c7025d80e6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 28, 2012
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 Code62032-514
Product Classification
G
Generic Name
Hydroquinone, Octinoxate,and Zinc Oxide
Product Specifications
Effective DateJanuary 10, 2013
FDA Product Classification