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Superlightener - 66915-413-17 - (Hydroquinone)

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Drug Information of Superlightener

Product NDC: 66915-413
Proprietary Name: Superlightener
Non Proprietary Name: Hydroquinone
Active Ingredient(s): 20    mg/g & nbsp;   Hydroquinone
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Superlightener

Product NDC: 66915-413
Labeler Name: CoValence Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part358A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100701

Package Information of Superlightener

Package NDC: 66915-413-17
Package Description: 30 g in 1 BOTTLE, GLASS (66915-413-17)

NDC Information of Superlightener

NDC Code 66915-413-17
Proprietary Name Superlightener
Package Description 30 g in 1 BOTTLE, GLASS (66915-413-17)
Product NDC 66915-413
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Hydroquinone
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100701
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name CoValence Inc
Substance Name HYDROQUINONE
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Superlightener


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