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Gillette Clinical
Gillette Clinical - 37000-780-14 - (Aluminum Zirconium Trichlorohydrex Gly)
Drug Information of Gillette Clinical
| Product NDC: | 37000-780 |
| 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: | 37000-780 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
Package Information of Gillette Clinical
| Package NDC: | 37000-780-14 |
| Package Description: | 1 CANISTER in 1 CARTON (37000-780-14) > 14 g in 1 CANISTER |
NDC Information of Gillette Clinical
| NDC Code | 37000-780-14 |
| Proprietary Name | Gillette Clinical |
| Package Description | 1 CANISTER in 1 CARTON (37000-780-14) > 14 g in 1 CANISTER |
| Product NDC | 37000-780 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Zirconium Trichlorohydrex Gly |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY |
| Strength Number | .2 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
