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DR.G WHITENING FORTIFIER - 51621-039-01 - (GLYCERIN)

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Drug Information of DR.G WHITENING FORTIFIER

Product NDC: 51621-039
Proprietary Name: DR.G WHITENING FORTIFIER
Non Proprietary Name: GLYCERIN
Active Ingredient(s): .15; 6    mL/30mL; mL/30mL & nbsp;   GLYCERIN
Administration Route(s): CUTANEOUS
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of DR.G WHITENING FORTIFIER

Product NDC: 51621-039
Labeler Name: GOWOONSESANG COSMETICS CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100601

Package Information of DR.G WHITENING FORTIFIER

Package NDC: 51621-039-01
Package Description: 30 mL in 1 CARTON (51621-039-01)

NDC Information of DR.G WHITENING FORTIFIER

NDC Code 51621-039-01
Proprietary Name DR.G WHITENING FORTIFIER
Package Description 30 mL in 1 CARTON (51621-039-01)
Product NDC 51621-039
Product Type Name HUMAN OTC DRUG
Non Proprietary Name GLYCERIN
Dosage Form Name CREAM
Route Name CUTANEOUS
Start Marketing Date 20100601
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name GOWOONSESANG COSMETICS CO., LTD.
Substance Name ALLANTOIN; GLYCERIN
Strength Number .15; 6
Strength Unit mL/30mL; mL/30mL
Pharmaceutical Classes

Complete Information of DR.G WHITENING FORTIFIER


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