Product NDC: | 51785-424 |
Proprietary Name: | Hand Sanitizer |
Non Proprietary Name: | BENZALKONIUM CHLORIDE |
Active Ingredient(s): | .0294 g/30mL & nbsp; BENZALKONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51785-424 |
Labeler Name: | Herbalife International of America Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120829 |
Package NDC: | 51785-424-01 |
Package Description: | 30 mL in 1 BOTTLE, SPRAY (51785-424-01) |
NDC Code | 51785-424-01 |
Proprietary Name | Hand Sanitizer |
Package Description | 30 mL in 1 BOTTLE, SPRAY (51785-424-01) |
Product NDC | 51785-424 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20120829 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Herbalife International of America Inc. |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .0294 |
Strength Unit | g/30mL |
Pharmaceutical Classes |