NDC 73823-051 Yoology Alcohol-free Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 73823-051?
What are the uses for Yoology Alcohol-free Hand Sanitizer?
Which are Yoology 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 Yoology 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:
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PURSLANE (UNII: M6S840WXG5)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- WATER (UNII: 059QF0KO0R)
- MINERAL OIL (UNII: T5L8T28FGP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALLANTOIN (UNII: 344S277G0Z)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Yoology Alcohol-free Hand Sanitizer?
- RxCUI: 2288822 - benzalkonium chloride 0.066 % Topical Lotion
- RxCUI: 2288822 - benzalkonium chloride 0.66 MG/ML Topical Lotion
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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".