| Product NDC: | 51614-0001 |
| Proprietary Name: | Ultracare For Hands |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | 1 mg/mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51614-0001 |
| Labeler Name: | Coltene Whaledent Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120622 |
| Package NDC: | 51614-0001-1 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (51614-0001-1) |
| NDC Code | 51614-0001-1 |
| Proprietary Name | Ultracare For Hands |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (51614-0001-1) |
| Product NDC | 51614-0001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120622 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Coltene Whaledent Inc |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |