| Product NDC: | 52138-200 |
| Proprietary Name: | TD Take Down Alcohol Free Antiseptic Hand Sanitizer |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .13 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52138-200 |
| Labeler Name: | Cleanphirst, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100331 |
| Package NDC: | 52138-200-17 |
| Package Description: | 50 mL in 1 BOTTLE (52138-200-17) |
| NDC Code | 52138-200-17 |
| Proprietary Name | TD Take Down Alcohol Free Antiseptic Hand Sanitizer |
| Package Description | 50 mL in 1 BOTTLE (52138-200-17) |
| Product NDC | 52138-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100331 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Cleanphirst, LLC |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .13 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |