| Product NDC: | 21749-607 |
| Proprietary Name: | PURELL SF607 Instant Hand Sanitizing |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .0013 mL/mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 21749-607 |
| Labeler Name: | GOJO Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110103 |
| Package NDC: | 21749-607-53 |
| Package Description: | 4 BOTTLE in 1 CASE (21749-607-53) > 535 mL in 1 BOTTLE |
| NDC Code | 21749-607-53 |
| Proprietary Name | PURELL SF607 Instant Hand Sanitizing |
| Package Description | 4 BOTTLE in 1 CASE (21749-607-53) > 535 mL in 1 BOTTLE |
| Product NDC | 21749-607 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110103 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GOJO Industries, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .0013 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |