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KLEENEX Alcohol Free Foam Hand Sanitizer - 55118-541-88 - (Benzalkonium Chloride)

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Drug Information of KLEENEX Alcohol Free Foam Hand Sanitizer

Product NDC: 55118-541
Proprietary Name: KLEENEX Alcohol Free Foam Hand Sanitizer
Non Proprietary Name: Benzalkonium Chloride
Active Ingredient(s): 1.3    mg/mL & nbsp;   Benzalkonium Chloride
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of KLEENEX Alcohol Free Foam Hand Sanitizer

Product NDC: 55118-541
Labeler Name: Kimberly-Clark Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130301

Package Information of KLEENEX Alcohol Free Foam Hand Sanitizer

Package NDC: 55118-541-88
Package Description: 236 mL in 1 BOTTLE, PLASTIC (55118-541-88)

NDC Information of KLEENEX Alcohol Free Foam Hand Sanitizer

NDC Code 55118-541-88
Proprietary Name KLEENEX Alcohol Free Foam Hand Sanitizer
Package Description 236 mL in 1 BOTTLE, PLASTIC (55118-541-88)
Product NDC 55118-541
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzalkonium Chloride
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20130301
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Kimberly-Clark Corporation
Substance Name BENZALKONIUM CHLORIDE
Strength Number 1.3
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of KLEENEX Alcohol Free Foam Hand Sanitizer


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