OBAGI-C RX SYSTEM NORMAL-OILY
OBAGI-C RX SYSTEM NORMAL-OILY SKIN INTERVENTION KIT
Approved
Approval ID
80cc66d6-325c-4203-bb11-e655939d8b46
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 2, 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 Code62032-517
Product Classification
G
Generic Name
HYDROQUINONE, OCTINOXATE AND ZINC OXIDE
Product Specifications
Effective DateJanuary 10, 2013
FDA Product Classification