NDC 82900-112 Magneleaf Cbd Thc
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82900 - M J Green Enterprises, Inc.
- 82900-112 - Magneleaf Cbd Thc
Product Characteristics
Product Packages
NDC Code 82900-112-13
Package Description: 170.96 g in 1 JAR
Product Details
What is NDC 82900-112?
What are the uses for Magneleaf Cbd Thc?
Which are Magneleaf Cbd Thc UNII Codes?
The UNII codes for the active ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- WATER (UNII: 059QF0KO0R) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- CANNABIDIOL (UNII: 19GBJ60SN5) (Active Moiety)
- MARANTA ARUNDINACEA ROOT (UNII: FVN346W31A)
- MARANTA ARUNDINACEA ROOT (UNII: FVN346W31A) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Magneleaf Cbd Thc 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:
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- COCONUT OIL (UNII: Q9L0O73W7L)
- PEG-8 BEESWAX (UNII: 3C1QUF1TIR)
- SHEA BUTTER (UNII: K49155WL9Y)
- JOJOBA OIL (UNII: 724GKU717M)
- .DELTA.9-TETRAHYDROCANNABINOL ACETATE (UNII: VHV54M2AES)
* 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".