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NeoStrata HQ Skin Lightening - 58414-8808-1 - (HYDROQUINONE)

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Drug Information of NeoStrata HQ Skin Lightening

Product NDC: 58414-8808
Proprietary Name: NeoStrata HQ Skin Lightening
Non Proprietary Name: HYDROQUINONE
Active Ingredient(s): .02    g/g & nbsp;   HYDROQUINONE
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of NeoStrata HQ Skin Lightening

Product NDC: 58414-8808
Labeler Name: NeoStrata Company Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part358A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110222

Package Information of NeoStrata HQ Skin Lightening

Package NDC: 58414-8808-1
Package Description: 1 TUBE in 1 CARTON (58414-8808-1) > 30 g in 1 TUBE

NDC Information of NeoStrata HQ Skin Lightening

NDC Code 58414-8808-1
Proprietary Name NeoStrata HQ Skin Lightening
Package Description 1 TUBE in 1 CARTON (58414-8808-1) > 30 g in 1 TUBE
Product NDC 58414-8808
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HYDROQUINONE
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20110222
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NeoStrata Company Inc
Substance Name HYDROQUINONE
Strength Number .02
Strength Unit g/g
Pharmaceutical Classes

Complete Information of NeoStrata HQ Skin Lightening


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