| Product NDC: | 37000-266 |
| Proprietary Name: | Gillette Clear Shield |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | .16 g/g & nbsp; Aluminum Chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37000-266 |
| Labeler Name: | Procter & Gamble Manufacturing Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
| Package NDC: | 37000-266-14 |
| Package Description: | 14 g in 1 CANISTER (37000-266-14) |
| NDC Code | 37000-266-14 |
| Proprietary Name | Gillette Clear Shield |
| Package Description | 14 g in 1 CANISTER (37000-266-14) |
| Product NDC | 37000-266 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Co. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | .16 |
| Strength Unit | g/g |
| Pharmaceutical Classes |