| Product NDC: | 57367-008 |
| Proprietary Name: | Anti-Perspirant Deodorant |
| Non Proprietary Name: | ALUMINUM CATION |
| Active Ingredient(s): | 52 mg/g & nbsp; ALUMINUM CATION |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 57367-008 |
| Labeler Name: | 220 Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100525 |
| Package NDC: | 57367-008-18 |
| Package Description: | 75 g in 1 TUBE (57367-008-18) |
| NDC Code | 57367-008-18 |
| Proprietary Name | Anti-Perspirant Deodorant |
| Package Description | 75 g in 1 TUBE (57367-008-18) |
| Product NDC | 57367-008 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CATION |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100525 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | 220 Laboratories Inc |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 52 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |