Product NDC: | 65517-1002 |
Proprietary Name: | DawnMist Antiperspirant Deodorant |
Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
Active Ingredient(s): | 79 mg/mL & nbsp; ALUMINUM CHLOROHYDRATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65517-1002 |
Labeler Name: | Dukal Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130110 |
Package NDC: | 65517-1002-2 |
Package Description: | 118 mL in 1 BOTTLE, PUMP (65517-1002-2) |
NDC Code | 65517-1002-2 |
Proprietary Name | DawnMist Antiperspirant Deodorant |
Package Description | 118 mL in 1 BOTTLE, PUMP (65517-1002-2) |
Product NDC | 65517-1002 |
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 | 79 |
Strength Unit | mg/mL |
Pharmaceutical Classes |