NDC 73143-010 Menthol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73143 - Jag Alliance, Llc
- 73143-010 - Menthol
Product Characteristics
Product Packages
NDC Code 73143-010-03
Package Description: 96 g in 1 CAN
Product Details
What is NDC 73143-010?
What are the uses for Menthol?
Which are Menthol UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
Which are Menthol 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:
- GLYCERETH-26 (UNII: NNE56F2N14)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- MENTHA ARVENSIS FLOWER OIL (UNII: Q129Z1W6Y2)
- ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- GLYCERIN (UNII: PDC6A3C0OX)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- MELALEUCA ALTERNIFOLIA FLOWERING TOP (UNII: 5AZ4S6N66F)
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE 1000 (UNII: MCU2324216)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- STEARIC ACID (UNII: 4ELV7Z65AP)
* Please review the disclaimer below.
[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".