| Product NDC: | 59779-252 | 
| Proprietary Name: | INSTANT FOAM HAND SANITIZER | 
| 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: | 59779-252 | 
| Labeler Name: | CVS PHARMACY | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part333E | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20110518 | 
| Package NDC: | 59779-252-02 | 
| Package Description: | 50 mL in 1 BOTTLE (59779-252-02) | 
| NDC Code | 59779-252-02 | 
| Proprietary Name | INSTANT FOAM HAND SANITIZER | 
| Package Description | 50 mL in 1 BOTTLE (59779-252-02) | 
| Product NDC | 59779-252 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | BENZALKONIUM CHLORIDE | 
| Dosage Form Name | GEL | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20110518 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | CVS PHARMACY | 
| Substance Name | BENZALKONIUM CHLORIDE | 
| Strength Number | .1 | 
| Strength Unit | mL/100mL | 
| Pharmaceutical Classes |