Product NDC: | 55118-560 |
Proprietary Name: | Kleenex Foam Antibacterial Skin Cleanser |
Non Proprietary Name: | Benzalkonium Chloride |
Active Ingredient(s): | .13 L/L & nbsp; Benzalkonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55118-560 |
Labeler Name: | Kimberly-Clark Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 55118-560-12 |
Package Description: | 1.2 L in 1 BOTTLE, PLASTIC (55118-560-12) |
NDC Code | 55118-560-12 |
Proprietary Name | Kleenex Foam Antibacterial Skin Cleanser |
Package Description | 1.2 L in 1 BOTTLE, PLASTIC (55118-560-12) |
Product NDC | 55118-560 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium Chloride |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Kimberly-Clark Corporation |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .13 |
Strength Unit | L/L |
Pharmaceutical Classes |