55118-700 NDC - KLEENEX ANTIMICROBIAL FOAM SKIN CLEANSER ()

Drug Information

Product NDC: 55118-700

Proprietary Name: KLEENEX Antimicrobial Foam Skin Cleanser

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Kimberly-Clark
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/1/2015

Package Information

No. Package Code Package Description Billing Unit
155118-700-18532 mL in 1 BOTTLE, PUMP (55118-700-18)
255118-700-636 CARTRIDGE in 1 CARTON (55118-700-63) / 1000 mL in 1 CARTRIDGE (55118-700-10)
355118-700-652 CARTRIDGE in 1 CARTON (55118-700-65) / 1200 mL in 1 CARTRIDGE (55118-700-12)
455118-700-662 BOTTLE, DISPENSING in 1 CARTON (55118-700-66) / 1500 mL in 1 BOTTLE, DISPENSING (55118-700-15)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55118-700The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEKLEENEX Antimicrobial Foam Skin CleanserThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/1/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEKimberly-ClarkName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023