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PF FOAMING ANTI-BACTERIAL HAND SANITIZING
PF FOAMING ANTI-BACTERIAL HAND SANITIZING - 76323-004-00 - (BENZALKONIUM CHLORIDE)
Drug Information of PF FOAMING ANTI-BACTERIAL HAND SANITIZING
| Product NDC: | 76323-004 |
| Proprietary Name: | PF FOAMING ANTI-BACTERIAL HAND SANITIZING |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .12 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PF FOAMING ANTI-BACTERIAL HAND SANITIZING
| Product NDC: | 76323-004 |
| Labeler Name: | Premium Formulations LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110701 |
Package Information of PF FOAMING ANTI-BACTERIAL HAND SANITIZING
| Package NDC: | 76323-004-00 |
| Package Description: | 250 mL in 1 BOTTLE (76323-004-00) |
NDC Information of PF FOAMING ANTI-BACTERIAL HAND SANITIZING
| NDC Code | 76323-004-00 |
| Proprietary Name | PF FOAMING ANTI-BACTERIAL HAND SANITIZING |
| Package Description | 250 mL in 1 BOTTLE (76323-004-00) |
| Product NDC | 76323-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | SOAP |
| 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 | mL/100mL |
| Pharmaceutical Classes |
