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CONDITION AND ENHANCE SYSTEM - 62032-508-04 - (HYDROQUINONE, OCTINOXATE AND ZINC OXIDE)

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Drug Information of CONDITION AND ENHANCE SYSTEM

Product NDC: 62032-508
Proprietary Name: CONDITION AND ENHANCE SYSTEM
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 CONDITION AND ENHANCE SYSTEM

Product NDC: 62032-508
Labeler Name: OMP, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20070820

Package Information of CONDITION AND ENHANCE SYSTEM

Package NDC: 62032-508-04
Package Description: 1 KIT in 1 CARTON (62032-508-04) * 60 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-118-36) * 60 mL in 1 BOTTLE, PLASTIC * 28.5 g in 1 BOTTLE, PLASTIC * 30 mL in 1 BOTTLE, PLASTIC (62032-119-10) * 57 g in 1 BOTTLE, PLASTIC (62032-117-36) * 28.5 g in 1 BOTTLE, PLASTIC (62032-115-10)

NDC Information of CONDITION AND ENHANCE SYSTEM

NDC Code 62032-508-04
Proprietary Name CONDITION AND ENHANCE SYSTEM
Package Description 1 KIT in 1 CARTON (62032-508-04) * 60 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-118-36) * 60 mL in 1 BOTTLE, PLASTIC * 28.5 g in 1 BOTTLE, PLASTIC * 30 mL in 1 BOTTLE, PLASTIC (62032-119-10) * 57 g in 1 BOTTLE, PLASTIC (62032-117-36) * 28.5 g in 1 BOTTLE, PLASTIC (62032-115-10)
Product NDC 62032-508
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROQUINONE, OCTINOXATE AND ZINC OXIDE
Dosage Form Name KIT
Route Name
Start Marketing Date 20070820
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name OMP, INC.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of CONDITION AND ENHANCE SYSTEM


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