Product NDC: | 10596-341 |
Proprietary Name: | Ban |
Non Proprietary Name: | ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY |
Active Ingredient(s): | 10.08 g/63g & nbsp; ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10596-341 |
Labeler Name: | Kao Brands Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111229 |
Package NDC: | 10596-341-22 |
Package Description: | 63 g in 1 CONTAINER (10596-341-22) |
NDC Code | 10596-341-22 |
Proprietary Name | Ban |
Package Description | 63 g in 1 CONTAINER (10596-341-22) |
Product NDC | 10596-341 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20111229 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kao Brands Company |
Substance Name | ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY |
Strength Number | 10.08 |
Strength Unit | g/63g |
Pharmaceutical Classes |