Product NDC: | 65517-1012 |
Proprietary Name: | DawnMist Antibacterial |
Non Proprietary Name: | TRICLOSAN |
Active Ingredient(s): | 3 mg/mL & nbsp; TRICLOSAN |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65517-1012 |
Labeler Name: | Dukal Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130110 |
Package NDC: | 65517-1012-1 |
Package Description: | 236 mL in 1 BOTTLE, PUMP (65517-1012-1) |
NDC Code | 65517-1012-1 |
Proprietary Name | DawnMist Antibacterial |
Package Description | 236 mL in 1 BOTTLE, PUMP (65517-1012-1) |
Product NDC | 65517-1012 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TRICLOSAN |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20130110 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Dukal Corporation |
Substance Name | TRICLOSAN |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes |