NDC 71023-445 Afia Alcohol-free Foaming Hand Sanitizer
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What is NDC 71023-445?
What are the uses for Afia Alcohol-free Foaming Hand Sanitizer?
Which are Afia Alcohol-free Foaming Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Afia Alcohol-free Foaming Hand Sanitizer 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:
- GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
- BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
- DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
- WATER (UNII: 059QF0KO0R)
- DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
What is the NDC to RxNorm Crosswalk for Afia Alcohol-free Foaming Hand Sanitizer?
- RxCUI: 1038799 - benzalkonium chloride 0.1 % Topical Foam
- RxCUI: 1038799 - benzalkonium chloride 1 MG/ML Topical Foam
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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".