Product NDC: | 53897-001 |
Proprietary Name: | Clinical Strength MiracleDry Antiperspirant Deodorant PM |
Non Proprietary Name: | ALUMINUM CHLORIDE |
Active Ingredient(s): | 12 mg/mL & nbsp; ALUMINUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53897-001 |
Labeler Name: | Highland Consumer Products |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121015 |
Package NDC: | 53897-001-01 |
Package Description: | 35.5 mL in 1 BOTTLE (53897-001-01) |
NDC Code | 53897-001-01 |
Proprietary Name | Clinical Strength MiracleDry Antiperspirant Deodorant PM |
Package Description | 35.5 mL in 1 BOTTLE (53897-001-01) |
Product NDC | 53897-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM CHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20121015 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Highland Consumer Products |
Substance Name | ALUMINUM CHLORIDE |
Strength Number | 12 |
Strength Unit | mg/mL |
Pharmaceutical Classes |