Product NDC: | 37000-288 |
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) |
Product NDC: | 37000-288 |
Labeler Name: | Procter and Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080501 |
Package NDC: | 37000-288-48 |
Package Description: | 1 CANISTER in 1 CARTON (37000-288-48) > 48 g in 1 CANISTER |
NDC Code | 37000-288-48 |
Proprietary Name | Gillette Clinical |
Package Description | 1 CANISTER in 1 CARTON (37000-288-48) > 48 g in 1 CANISTER |
Product NDC | 37000-288 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20080501 |
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 |