| Product NDC: | 76118-0001 |
| Proprietary Name: | PURAX PURE PADS |
| Non Proprietary Name: | Aluminum Chloride |
| Active Ingredient(s): | 50 mL/7.5mL & nbsp; Aluminum Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76118-0001 |
| Labeler Name: | Purax International GmbH |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110328 |
| Package NDC: | 76118-0001-1 |
| Package Description: | 50 mL in 1 BOTTLE, SPRAY (76118-0001-1) |
| NDC Code | 76118-0001-1 |
| Proprietary Name | PURAX PURE PADS |
| Package Description | 50 mL in 1 BOTTLE, SPRAY (76118-0001-1) |
| Product NDC | 76118-0001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chloride |
| Dosage Form Name | AEROSOL, SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20110328 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Purax International GmbH |
| Substance Name | ALUMINUM CHLORIDE |
| Strength Number | 50 |
| Strength Unit | mL/7.5mL |
| Pharmaceutical Classes |