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Gillette Clinical - 37000-287-48 - (Aluminum Zirconium Trichlorohydrex Gly)

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Drug Information of Gillette Clinical

Product NDC: 37000-287
Proprietary Name: Gillette Clinical
Non Proprietary Name: Aluminum Zirconium Trichlorohydrex Gly
Active Ingredient(s): .2    g/g & nbsp;   Aluminum Zirconium Trichlorohydrex Gly
Administration Route(s): TOPICAL
Dosage Form(s): STICK
Coding System: National Drug Codes(NDC)

Labeler Information of Gillette Clinical

Product NDC: 37000-287
Labeler Name: Procter and Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part350
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20071201

Package Information of Gillette Clinical

Package NDC: 37000-287-48
Package Description: 1 CANISTER in 1 CARTON (37000-287-48) > 48 g in 1 CANISTER

NDC Information of Gillette Clinical

NDC Code 37000-287-48
Proprietary Name Gillette Clinical
Package Description 1 CANISTER in 1 CARTON (37000-287-48) > 48 g in 1 CANISTER
Product NDC 37000-287
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aluminum Zirconium Trichlorohydrex Gly
Dosage Form Name STICK
Route Name TOPICAL
Start Marketing Date 20071201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Procter and Gamble Manufacturing Company
Substance Name ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Strength Number .2
Strength Unit g/g
Pharmaceutical Classes

Complete Information of Gillette Clinical


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