| Product NDC: | 13537-427 |
| Proprietary Name: | LBEL |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | .24 g/mL & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 13537-427 |
| Labeler Name: | Ventura Corporation Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120120 |
| Package NDC: | 13537-427-01 |
| Package Description: | 125 mL in 1 CAN (13537-427-01) |
| NDC Code | 13537-427-01 |
| Proprietary Name | LBEL |
| Package Description | 125 mL in 1 CAN (13537-427-01) |
| Product NDC | 13537-427 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
| Dosage Form Name | AEROSOL, SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20120120 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura Corporation Ltd |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | .24 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |