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OBAGI-C RX SYSTEM NORMAL-DRY - 62032-518-04 - (HYDROQUINONE, OCTINOXATE AND ZINC OXIDE)

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Drug Information of OBAGI-C RX SYSTEM NORMAL-DRY

Product NDC: 62032-518
Proprietary Name: OBAGI-C RX SYSTEM NORMAL-DRY
Non Proprietary Name: HYDROQUINONE, OCTINOXATE AND ZINC OXIDE
Active Ingredient(s):    & nbsp;   HYDROQUINONE, OCTINOXATE AND ZINC OXIDE
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of OBAGI-C RX SYSTEM NORMAL-DRY

Product NDC: 62032-518
Labeler Name: OMP, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20121107

Package Information of OBAGI-C RX SYSTEM NORMAL-DRY

Package NDC: 62032-518-04
Package Description: 1 KIT in 1 CARTON (62032-518-04) * 85 g in 1 TUBE (62032-121-90) * 177 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-105-36) * 1 BOTTLE, GLASS in 1 CARTON (62032-106-10) > 30 mL in 1 BOTTLE, GLASS

NDC Information of OBAGI-C RX SYSTEM NORMAL-DRY

NDC Code 62032-518-04
Proprietary Name OBAGI-C RX SYSTEM NORMAL-DRY
Package Description 1 KIT in 1 CARTON (62032-518-04) * 85 g in 1 TUBE (62032-121-90) * 177 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-105-36) * 1 BOTTLE, GLASS in 1 CARTON (62032-106-10) > 30 mL in 1 BOTTLE, GLASS
Product NDC 62032-518
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROQUINONE, OCTINOXATE AND ZINC OXIDE
Dosage Form Name KIT
Route Name
Start Marketing Date 20121107
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name OMP, INC.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of OBAGI-C RX SYSTEM NORMAL-DRY


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