NDC 55118-700 Kleenex Antimicrobial Foam Skin Cleanser

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
55118-700
Proprietary Name:
Kleenex Antimicrobial Foam Skin Cleanser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
55118
Start Marketing Date: [9]
09-01-2015
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 55118-700?

The NDC code 55118-700 is assigned by the FDA to the product Kleenex Antimicrobial Foam Skin Cleanser which is product labeled by Kimberly-clark. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 55118-700-18 532 ml in 1 bottle, pump , 55118-700-63 6 cartridge in 1 carton / 1000 ml in 1 cartridge (55118-700-10), 55118-700-65 2 cartridge in 1 carton / 1200 ml in 1 cartridge (55118-700-12), 55118-700-66 2 bottle, dispensing in 1 carton / 1500 ml in 1 bottle, dispensing (55118-700-15). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Kleenex Antimicrobial Foam Skin Cleanser?

Apply a small amount and lather hands in water for at least 30 seconds. Rinse well. Adults: Supervise children when using this product. Do not dilute product. For occasional use as needed.

Which are Kleenex Antimicrobial Foam Skin Cleanser UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Kleenex Antimicrobial Foam Skin Cleanser Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".