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KLEENEX Antimicrobial Foam Skin Cleanser - 55118-440-15 - (Benzalkonium Chloride)

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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: 55118-440-15
Package Description: 1.5 L in 1 BOTTLE, PLASTIC (55118-440-15)

NDC Information of KLEENEX Antimicrobial Foam Skin Cleanser

NDC Code 55118-440-15
Proprietary Name KLEENEX Antimicrobial Foam Skin Cleanser
Package Description 1.5 L in 1 BOTTLE, PLASTIC (55118-440-15)
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

Complete Information of KLEENEX Antimicrobial Foam Skin Cleanser


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