Product NDC: | 54913-001 |
Proprietary Name: | SWEATBLOCK |
Non Proprietary Name: | ALUMINUM CHLORIDE |
Active Ingredient(s): | 14 mL/100mL & nbsp; ALUMINUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54913-001 |
Labeler Name: | DC Alpine Partners, LLC DBA: Sweatblock |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111026 |
Package NDC: | 54913-001-08 |
Package Description: | 8 PACKET in 1 BOX (54913-001-08) > 2.6 mL in 1 PACKET |
NDC Code | 54913-001-08 |
Proprietary Name | SWEATBLOCK |
Package Description | 8 PACKET in 1 BOX (54913-001-08) > 2.6 mL in 1 PACKET |
Product NDC | 54913-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM CHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20111026 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DC Alpine Partners, LLC DBA: Sweatblock |
Substance Name | ALUMINUM CHLORIDE |
Strength Number | 14 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |