NDC 72288-752 Amazon Commercial Alcohol Free Foam Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72288 - Amazon.com Services
- 72288-752 - Amazon Commercial Alcohol Free Foam Hand Sanitizer
Product Packages
NDC Code 72288-752-04
Package Description: 3870 mL in 1 JUG
Product Details
What is NDC 72288-752?
What are the uses for Amazon Commercial Alcohol Free Foam Hand Sanitizer?
Which are Amazon Commercial Alcohol Free Foam 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 Amazon Commercial Alcohol Free Foam 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:
- GERANIOL (UNII: L837108USY)
- SODIUM PIDOLATE (UNII: 1V74VH163T)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- PEG/PPG-15/15 ALLYL ETHER ACETATE (UNII: 8RP39FN7AJ)
- PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
- N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)
- ORANGE OIL (UNII: AKN3KSD11B)
- .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
- DIOXANE (UNII: J8A3S10O7S)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- HEXYL SALICYLATE (UNII: 8F78EY72YL)
- ALCOHOL (UNII: 3K9958V90M)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ACETALDEHYDE (UNII: GO1N1ZPR3B)
- LIME OIL (UNII: UZH29XGA8G)
- LEMON OIL (UNII: I9GRO824LL)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)
- MYRCENE (UNII: 3M39CZS25B)
- DIHYDROMYRCENOL (UNII: 46L1B02ND9)
- METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- WATER (UNII: 059QF0KO0R)
- D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
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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".