NDC 82697-221 Anti-bacterial Dayoff Hand Sanitizer
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What is NDC 82697-221?
What are the uses for Anti-bacterial Dayoff Hand Sanitizer?
Which are Anti-bacterial Dayoff Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Anti-bacterial Dayoff 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ULTRAMARINE BLUE (UNII: I39WR998BI)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Anti-bacterial Dayoff Hand Sanitizer?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 ML/ML Topical Gel
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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".