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 |