Product NDC: | 50730-5101 |
Proprietary Name: | BZK Antiseptic Towelette |
Non Proprietary Name: | benzalkonium chloride |
Active Ingredient(s): | .0013 mL/1 & nbsp; benzalkonium chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50730-5101 |
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: | 19971017 |
Package NDC: | 50730-5101-0 |
Package Description: | 100 PACKET in 1 CARTON (50730-5101-0) > 1 SOLUTION in 1 PACKET |
NDC Code | 50730-5101-0 |
Proprietary Name | BZK Antiseptic Towelette |
Package Description | 100 PACKET in 1 CARTON (50730-5101-0) > 1 SOLUTION in 1 PACKET |
Product NDC | 50730-5101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | benzalkonium chloride |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19971017 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | H and P Industries, Inc. dba Triad Group |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .0013 |
Strength Unit | mL/1 |
Pharmaceutical Classes |