| Product NDC: | 49967-272 |
| Proprietary Name: | Kiehls Since 1851 CrossTerrain Antiperspirant Deodorant |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | 15 g/75g & nbsp; Aluminum Chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49967-272 |
| Labeler Name: | L'Oreal USA Products Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
| Package NDC: | 49967-272-01 |
| Package Description: | 75 g in 1 CONTAINER (49967-272-01) |
| NDC Code | 49967-272-01 |
| Proprietary Name | Kiehls Since 1851 CrossTerrain Antiperspirant Deodorant |
| Package Description | 75 g in 1 CONTAINER (49967-272-01) |
| Product NDC | 49967-272 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 15 |
| Strength Unit | g/75g |
| Pharmaceutical Classes |