NDC 77419-4000 Amass Lemon Tisane Botanic Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77419 - Amass Brands, Inc
- 77419-4000 - Amass Lemon Tisane Botanic Hand Sanitizer
Product Packages
NDC Code 77419-4000-1
Package Description: 3.785 L in 1 BOTTLE, PUMP
NDC Code 77419-4000-2
Package Description: 1.893 L in 1 BOTTLE, PUMP
Product Details
What is NDC 77419-4000?
What are the uses for Amass Lemon Tisane Botanic Hand Sanitizer?
Which are Amass Lemon Tisane Botanic 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 Amass Lemon Tisane Botanic 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:
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- CEDRUS ATLANTICA BARK OIL (UNII: ZX5QRE4U60)
- WATER (UNII: 059QF0KO0R)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- LEMON OIL (UNII: I9GRO824LL)
- GINGER OIL (UNII: SAS9Z1SVUK)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- SANDALWOOD OIL (UNII: X7X01WMQ5F)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- HYDROXYPROPYL CELLULOSE (90000 WAMW) (UNII: UKE75GEA7F)
- CETYL LACTATE (UNII: A7EVH2RK4O)
- MYRISTYL LACTATE (UNII: 1D822OC34X)
- GLYCEROL FORMAL (UNII: 3L7GR2604E)
- BENZYL BENZOATE (UNII: N863NB338G)
- METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
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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".