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ZeroSweat
ZeroSweat - 55726-048-01 - (Aluminum Chloride)
Drug Information of ZeroSweat
| Product NDC: | 55726-048 |
| Proprietary Name: | ZeroSweat |
| Non Proprietary Name: | Aluminum Chloride |
| Active Ingredient(s): | 15 mg/mL & nbsp; Aluminum Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZeroSweat
| Product NDC: | 55726-048 |
| Labeler Name: | ZeroSweat Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120611 |
Package Information of ZeroSweat
| Package NDC: | 55726-048-01 |
| Package Description: | 35.5 mL in 1 BOTTLE (55726-048-01) |
NDC Information of ZeroSweat
| NDC Code | 55726-048-01 |
| Proprietary Name | ZeroSweat |
| Package Description | 35.5 mL in 1 BOTTLE (55726-048-01) |
| Product NDC | 55726-048 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120611 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ZeroSweat Inc |
| Substance Name | ALUMINUM CHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
