| Product NDC: | 29500-9088 |
| Proprietary Name: | Hand Sanitizer |
| Non Proprietary Name: | benzalkonium chloride |
| Active Ingredient(s): | .27 mL/207mL & nbsp; benzalkonium chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 29500-9088 |
| Labeler Name: | Personal Care Products |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110705 |
| Package NDC: | 29500-9088-7 |
| Package Description: | 207 mL in 1 BOTTLE, PLASTIC (29500-9088-7) |
| NDC Code | 29500-9088-7 |
| Proprietary Name | Hand Sanitizer |
| Package Description | 207 mL in 1 BOTTLE, PLASTIC (29500-9088-7) |
| Product NDC | 29500-9088 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzalkonium chloride |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110705 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Personal Care Products |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .27 |
| Strength Unit | mL/207mL |
| Pharmaceutical Classes |