NDC 55118-571 Kleenex Antiseptic Skin Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55118 - Kimberly-clark
- 55118-571 - Kleenex Antiseptic Skin Cleanser
Product Packages
NDC Code 55118-571-63
Package Description: 6 CONTAINER in 1 CARTON / 1 L in 1 CONTAINER (55118-571-10)
NDC Code 55118-571-65
Package Description: 2 CONTAINER in 1 CARTON / 1.2 L in 1 CONTAINER (55118-571-12)
Product Details
What is NDC 55118-571?
What are the uses for Kleenex Antiseptic Skin Cleanser?
Which are Kleenex Antiseptic Skin Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Kleenex Antiseptic 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:
- WATER (UNII: 059QF0KO0R)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Kleenex Antiseptic Skin Cleanser?
- RxCUI: 1053758 - chloroxylenol 1.75 % Medicated Liquid Soap
- RxCUI: 1053758 - chloroxylenol 17.5 MG/ML Medicated Liquid Soap
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[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".