NDC 63824-479 Lysol No-touch
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63824-479?
What are the uses for Lysol No-touch?
Which are Lysol No-touch UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Lysol No-touch 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)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PPG-12-BUTETH-16 (UNII: 58CG7042J1)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Lysol No-touch?
- RxCUI: 1233282 - benzalkonium chloride 0.1 % Medicated Liquid Soap
- RxCUI: 1233282 - benzalkonium chloride 1 MG/ML Medicated Liquid Soap
- RxCUI: 1429887 - Lysol No-Touch 0.1 % Medicated Liquid Soap
- RxCUI: 1429887 - benzalkonium chloride 1 MG/ML Medicated Liquid Soap [Lysol No-Touch Hand Soap]
- RxCUI: 1429887 - Lysol No-Touch Hand Soap 0.1 % 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".