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 |