NDC 72593-158 Cbd Menthol Pain Relief Fast Acting Pain Roller
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72593 - Global Products Group, Llc
- 72593-158 - Cbd Menthol Pain Relief
Product Packages
NDC Code 72593-158-12
Package Description: 88 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 72593-158?
What are the uses for Cbd Menthol Pain Relief Fast Acting Pain Roller?
Which are Cbd Menthol Pain Relief Fast Acting Pain Roller 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 Cbd Menthol Pain Relief Fast Acting Pain Roller 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)
- GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N)
- GLYCERIN (UNII: PDC6A3C0OX)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
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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".