| 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 |