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Ban - 10596-339-35 - (Aluminum Chlorohydrate)
Drug Information of Ban
| Product NDC: | 10596-339 |
| 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) |
Labeler Information of Ban
| Product NDC: | 10596-339 |
| Labeler Name: | Kao Brands Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120101 |
Package Information of Ban
| Package NDC: | 10596-339-35 |
| Package Description: | 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-339-35) |
NDC Information of Ban
| NDC Code | 10596-339-35 |
| Proprietary Name | Ban |
| Package Description | 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-339-35) |
| Product NDC | 10596-339 |
| 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 |
