Product NDC: | 76118-0002 |
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): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76118-0002 |
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: | 76118-0002-1 |
Package Description: | 50 mL in 1 BOTTLE, WITH APPLICATOR (76118-0002-1) |
NDC Code | 76118-0002-1 |
Proprietary Name | PURAX PURE PADS |
Package Description | 50 mL in 1 BOTTLE, WITH APPLICATOR (76118-0002-1) |
Product NDC | 76118-0002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aluminum Chloride |
Dosage Form Name | LIQUID |
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 |