Home > National Drug Code (NDC) > OBAGI C RX SYSTEM C CLARIFYING SERUM

OBAGI C RX SYSTEM C CLARIFYING SERUM - 62032-122-10 - (HYDROQUINONE)

Alphabetical Index


Drug Information of OBAGI C RX SYSTEM C CLARIFYING SERUM

Product NDC: 62032-122
Proprietary Name: OBAGI C RX SYSTEM C CLARIFYING SERUM
Non Proprietary Name: HYDROQUINONE
Active Ingredient(s): 40    mg/mL & nbsp;   HYDROQUINONE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of OBAGI C RX SYSTEM C CLARIFYING SERUM

Product NDC: 62032-122
Labeler Name: OMP, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100101

Package Information of OBAGI C RX SYSTEM C CLARIFYING SERUM

Package NDC: 62032-122-10
Package Description: 1 BOTTLE, GLASS in 1 CARTON (62032-122-10) > 30 mL in 1 BOTTLE, GLASS

NDC Information of OBAGI C RX SYSTEM C CLARIFYING SERUM

NDC Code 62032-122-10
Proprietary Name OBAGI C RX SYSTEM C CLARIFYING SERUM
Package Description 1 BOTTLE, GLASS in 1 CARTON (62032-122-10) > 30 mL in 1 BOTTLE, GLASS
Product NDC 62032-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROQUINONE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name OMP, INC.
Substance Name HYDROQUINONE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA]

Complete Information of OBAGI C RX SYSTEM C CLARIFYING SERUM


General Information