NDC 64483-492 Hemp Theory Fast Acting Pain
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64483 - Clientele, Inc.
- 64483-492 - Hemp Theory
Product Characteristics
Product Packages
NDC Code 64483-492-03
Package Description: 89 mL in 1 TUBE
Product Details
What is NDC 64483-492?
What are the uses for Hemp Theory Fast Acting Pain?
Which are Hemp Theory Fast Acting Pain 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 Hemp Theory Fast Acting Pain 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:
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCOL STEARATE SE (UNII: 6YLY96TQL6)
- APOCYNUM CANNABINUM ROOT (UNII: 2F92409L9Z)
- BETADEX (UNII: JV039JZZ3A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- COCONUT OIL (UNII: Q9L0O73W7L)
- N-ACETYLGLUCOSAMINE (UNII: V956696549)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- 1-(4-HYDROXY-3-METHOXYPHENYL)-DECAN-3-ONE (UNII: BO24ID7E9U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TURMERIC (UNII: 856YO1Z64F)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- C20-40 PARETH-3 (UNII: 68103A23TQ)
- ASTAXANTHIN (UNII: 8XPW32PR7I)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TROLAMINE (UNII: 9O3K93S3TK)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
* 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".