| Product NDC: | 76323-001 |
| Proprietary Name: | PF ANTI-BACTERIAL HAND SANITIZING WIPES |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .12 g/100g & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76323-001 |
| Labeler Name: | Premium Formulations LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110701 |
| Package NDC: | 76323-001-00 |
| Package Description: | 4.7 g in 1 PACKAGE (76323-001-00) |
| NDC Code | 76323-001-00 |
| Proprietary Name | PF ANTI-BACTERIAL HAND SANITIZING WIPES |
| Package Description | 4.7 g in 1 PACKAGE (76323-001-00) |
| Product NDC | 76323-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Premium Formulations LLC |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .12 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |