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Gillette Clear
Gillette Clear - 37000-268-30 - (Aluminum Zirconium Octachlorohydrex Gly)
Drug Information of Gillette Clear
| Product NDC: | 37000-268 |
| Proprietary Name: | Gillette Clear |
| Non Proprietary Name: | Aluminum Zirconium Octachlorohydrex Gly |
| Active Ingredient(s): | .16 g/g & nbsp; Aluminum Zirconium Octachlorohydrex Gly |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gillette Clear
| Product NDC: | 37000-268 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080501 |
Package Information of Gillette Clear
| Package NDC: | 37000-268-30 |
| Package Description: | 85 g in 1 CANISTER (37000-268-30) |
NDC Information of Gillette Clear
| NDC Code | 37000-268-30 |
| Proprietary Name | Gillette Clear |
| Package Description | 85 g in 1 CANISTER (37000-268-30) |
| Product NDC | 37000-268 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Zirconium Octachlorohydrex Gly |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20080501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY |
| Strength Number | .16 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
