Product NDC: | 10596-337 |
Proprietary Name: | Ban |
Non Proprietary Name: | Aluminum Chlorohydrate |
Active Ingredient(s): | 20 g/103mL & nbsp; Aluminum Chlorohydrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10596-337 |
Labeler Name: | Kao Brands Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120101 |
Package NDC: | 10596-337-35 |
Package Description: | 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-337-35) |
NDC Code | 10596-337-35 |
Proprietary Name | Ban |
Package Description | 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-337-35) |
Product NDC | 10596-337 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aluminum Chlorohydrate |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kao Brands Company |
Substance Name | ALUMINUM CHLOROHYDRATE |
Strength Number | 20 |
Strength Unit | g/103mL |
Pharmaceutical Classes |