| Product NDC: | 76273-001 |
| Proprietary Name: | Antibacterial Hand |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .1 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76273-001 |
| Labeler Name: | MAYBORN USA, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110727 |
| Package NDC: | 76273-001-01 |
| Package Description: | 50 mL in 1 BOTTLE, PLASTIC (76273-001-01) |
| NDC Code | 76273-001-01 |
| Proprietary Name | Antibacterial Hand |
| Package Description | 50 mL in 1 BOTTLE, PLASTIC (76273-001-01) |
| Product NDC | 76273-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110727 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MAYBORN USA, INC. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |