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DawnMist Antiperspirant Deodorant
DawnMist Antiperspirant Deodorant - 65517-1010-1 - (ALUMINUM CHLOROHYDRATE)
Drug Information of DawnMist Antiperspirant Deodorant
| Product NDC: | 65517-1010 |
| Proprietary Name: | DawnMist Antiperspirant Deodorant |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | 78 mg/mL & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DawnMist Antiperspirant Deodorant
| Product NDC: | 65517-1010 |
| Labeler Name: | Dukal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130110 |
Package Information of DawnMist Antiperspirant Deodorant
| Package NDC: | 65517-1010-1 |
| Package Description: | 44 mL in 1 BOTTLE, WITH APPLICATOR (65517-1010-1) |
NDC Information of DawnMist Antiperspirant Deodorant
| NDC Code | 65517-1010-1 |
| Proprietary Name | DawnMist Antiperspirant Deodorant |
| Package Description | 44 mL in 1 BOTTLE, WITH APPLICATOR (65517-1010-1) |
| Product NDC | 65517-1010 |
| 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 | 78 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
