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 |