| Product NDC: | 65517-1004 |
| 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: | 65517-1004 |
| Labeler Name: | Dukal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130110 |
| Package NDC: | 65517-1004-1 |
| Package Description: | 44 mL in 1 BOTTLE, WITH APPLICATOR (65517-1004-1) |
| NDC Code | 65517-1004-1 |
| Proprietary Name | DawnMist Antiperspirant Deodorant |
| Package Description | 44 mL in 1 BOTTLE, WITH APPLICATOR (65517-1004-1) |
| Product NDC | 65517-1004 |
| 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 |