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Dermaclair Skin Lightening - 66619-131-31 - (HYDROQUINONE)

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Drug Information of Dermaclair Skin Lightening

Product NDC: 66619-131
Proprietary Name: Dermaclair Skin Lightening
Non Proprietary Name: HYDROQUINONE
Active Ingredient(s): 1; .25    g/50g; g/50g & nbsp;   HYDROQUINONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Dermaclair Skin Lightening

Product NDC: 66619-131
Labeler Name: International Beauty Exchange
Product Type: HUMAN OTC DRUG
FDA Application Number: part358A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110101

Package Information of Dermaclair Skin Lightening

Package NDC: 66619-131-31
Package Description: 50 g in 1 TUBE (66619-131-31)

NDC Information of Dermaclair Skin Lightening

NDC Code 66619-131-31
Proprietary Name Dermaclair Skin Lightening
Package Description 50 g in 1 TUBE (66619-131-31)
Product NDC 66619-131
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HYDROQUINONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name International Beauty Exchange
Substance Name HYDROQUINONE; OCTINOXATE
Strength Number 1; .25
Strength Unit g/50g; g/50g
Pharmaceutical Classes

Complete Information of Dermaclair Skin Lightening


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