Product NDC: | 10685-681 |
Proprietary Name: | Carroll Ultrex Antimicrobial Wipes |
Non Proprietary Name: | Benzalkonium Chloride |
Active Ingredient(s): | .01417 g/1 & nbsp; Benzalkonium Chloride |
Administration Route(s): | PERCUTANEOUS |
Dosage Form(s): | CLOTH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10685-681 |
Labeler Name: | Carroll Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120915 |
Package NDC: | 10685-681-97 |
Package Description: | 70 CLOTH in 1 CANISTER (10685-681-97) |
NDC Code | 10685-681-97 |
Proprietary Name | Carroll Ultrex Antimicrobial Wipes |
Package Description | 70 CLOTH in 1 CANISTER (10685-681-97) |
Product NDC | 10685-681 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium Chloride |
Dosage Form Name | CLOTH |
Route Name | PERCUTANEOUS |
Start Marketing Date | 20120915 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Carroll Company |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .01417 |
Strength Unit | g/1 |
Pharmaceutical Classes |