Product NDC: | 50730-1001 |
Proprietary Name: | Cold Sore Treatment |
Non Proprietary Name: | Benzalkonium Chloride |
Active Ingredient(s): | .13 mL/mL & nbsp; Benzalkonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | TINCTURE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50730-1001 |
Labeler Name: | H and P Industries, Inc. dba Triad Group |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20070601 |
Package NDC: | 50730-1001-1 |
Package Description: | 2 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (50730-1001-1) > .6 mL in 1 VIAL, PATENT DELIVERY SYSTEM |
NDC Code | 50730-1001-1 |
Proprietary Name | Cold Sore Treatment |
Package Description | 2 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (50730-1001-1) > .6 mL in 1 VIAL, PATENT DELIVERY SYSTEM |
Product NDC | 50730-1001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium Chloride |
Dosage Form Name | TINCTURE |
Route Name | TOPICAL |
Start Marketing Date | 20070601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | H and P Industries, Inc. dba Triad Group |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .13 |
Strength Unit | mL/mL |
Pharmaceutical Classes |