Product NDC: | 65517-1005 |
Proprietary Name: | DawnMist Antiperspirant Deodorant |
Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
Active Ingredient(s): | 45 mg/mL & nbsp; ALUMINUM CHLOROHYDRATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65517-1005 |
Labeler Name: | Dukal Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130110 |
Package NDC: | 65517-1005-1 |
Package Description: | 59 mL in 1 BOTTLE, WITH APPLICATOR (65517-1005-1) |
NDC Code | 65517-1005-1 |
Proprietary Name | DawnMist Antiperspirant Deodorant |
Package Description | 59 mL in 1 BOTTLE, WITH APPLICATOR (65517-1005-1) |
Product NDC | 65517-1005 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130110 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dukal Corporation |
Substance Name | ALUMINUM CHLOROHYDRATE |
Strength Number | 45 |
Strength Unit | mg/mL |
Pharmaceutical Classes |