NDC 74538-0007 Folks Alcohol Free Hand Sanitizer
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What is NDC 74538-0007?
What are the uses for Folks Alcohol Free Hand Sanitizer?
Which are Folks Alcohol Free 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 Folks Alcohol Free 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:
- WATER (UNII: 059QF0KO0R)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
What is the NDC to RxNorm Crosswalk for Folks Alcohol Free Hand Sanitizer?
- RxCUI: 1052947 - benzalkonium chloride 0.1 % Topical Spray
- RxCUI: 1052947 - benzalkonium chloride 1 MG/ML Topical Spray
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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".