Product NDC: | 66774-1003 |
Proprietary Name: | Viroxyn Professional Use |
Non Proprietary Name: | Benzalkonium chloride and Benzocaine |
Active Ingredient(s): | 1.14; 65.775 mg/mL; mg/mL & nbsp; Benzalkonium chloride and Benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66774-1003 |
Labeler Name: | Quadex Pharmaceuticals LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121022 |
Package NDC: | 66774-1003-5 |
Package Description: | 12 AMPULE in 1 BLISTER PACK (66774-1003-5) > .6 mL in 1 AMPULE |
NDC Code | 66774-1003-5 |
Proprietary Name | Viroxyn Professional Use |
Package Description | 12 AMPULE in 1 BLISTER PACK (66774-1003-5) > .6 mL in 1 AMPULE |
Product NDC | 66774-1003 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium chloride and Benzocaine |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20121022 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Quadex Pharmaceuticals LLC |
Substance Name | BENZALKONIUM CHLORIDE; BENZOCAINE |
Strength Number | 1.14; 65.775 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |