| Product NDC: | 51053-500 |
| Proprietary Name: | Alcohol free hand sanitizer |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | 1.2 mL/1000mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51053-500 |
| Labeler Name: | Sanihealth Products Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100524 |
| Package NDC: | 51053-500-10 |
| Package Description: | 1000 mL in 1 BOTTLE, PUMP (51053-500-10) |
| NDC Code | 51053-500-10 |
| Proprietary Name | Alcohol free hand sanitizer |
| Package Description | 1000 mL in 1 BOTTLE, PUMP (51053-500-10) |
| Product NDC | 51053-500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100524 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sanihealth Products Corporation |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.2 |
| Strength Unit | mL/1000mL |
| Pharmaceutical Classes |