NDC 80078-001 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 80078-001?
What are the uses for Hand Sanitizer?
Which are Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are 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:
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- SPEARMINT OIL (UNII: C3M81465G5)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- 2-AMINO-1,3-PROPANEDIOL (UNII: IC94L30J8M)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- RHODIOLA ROSEA ROOT (UNII: 3S5ITS5ULN)
- VACCINIUM ANGUSTIFOLIUM WHOLE (UNII: R3538BZ1BW)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SAGE OIL (UNII: U27K0H1H2O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PANTHENOL (UNII: WV9CM0O67Z)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- COCO GLUCOSIDE (UNII: ICS790225B)
- SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
- ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)
- BETAINE (UNII: 3SCV180C9W)
- WITCH HAZEL (UNII: 101I4J0U34)
- CEDRUS ATLANTICA BARK OIL (UNII: ZX5QRE4U60)
- VANILLA PLANIFOLIA OIL (UNII: 0A3F415158)
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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".