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balance-n-brighten - 51389-104-01 - (TITANIUM DIOXIDE)

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Drug Information of balance-n-brighten

Product NDC: 51389-104
Proprietary Name: balance-n-brighten
Non Proprietary Name: TITANIUM DIOXIDE
Active Ingredient(s): 10    g/100g & nbsp;   TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of balance-n-brighten

Product NDC: 51389-104
Labeler Name: LAURA GELLER MAKE UP INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20111113

Package Information of balance-n-brighten

Package NDC: 51389-104-01
Package Description: 1 CONTAINER in 1 KIT (51389-104-01) > 9 g in 1 CONTAINER

NDC Information of balance-n-brighten

NDC Code 51389-104-01
Proprietary Name balance-n-brighten
Package Description 1 CONTAINER in 1 KIT (51389-104-01) > 9 g in 1 CONTAINER
Product NDC 51389-104
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TITANIUM DIOXIDE
Dosage Form Name POWDER
Route Name TOPICAL
Start Marketing Date 20111113
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name LAURA GELLER MAKE UP INC.
Substance Name TITANIUM DIOXIDE
Strength Number 10
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of balance-n-brighten


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