Home
>
National Drug Code (NDC)
>
KLEENEX Antimicrobial Foam Skin Cleanser
KLEENEX Antimicrobial Foam Skin Cleanser - 55118-440-12 - (Benzalkonium Chloride)
Drug Information of KLEENEX Antimicrobial Foam Skin Cleanser
| Product NDC: | 55118-440 |
| Proprietary Name: | KLEENEX Antimicrobial Foam Skin Cleanser |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .013 mg/L & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KLEENEX Antimicrobial Foam Skin Cleanser
| Product NDC: | 55118-440 |
| Labeler Name: | Kimberly-Clark Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130620 |
Package Information of KLEENEX Antimicrobial Foam Skin Cleanser
| Package NDC: | 55118-440-12 |
| Package Description: | 1.2 L in 1 BOTTLE, PLASTIC (55118-440-12) |
NDC Information of KLEENEX Antimicrobial Foam Skin Cleanser
| NDC Code | 55118-440-12 |
| Proprietary Name | KLEENEX Antimicrobial Foam Skin Cleanser |
| Package Description | 1.2 L in 1 BOTTLE, PLASTIC (55118-440-12) |
| Product NDC | 55118-440 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130620 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kimberly-Clark Corporation |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .013 |
| Strength Unit | mg/L |
| Pharmaceutical Classes |
