NDC 52261-4901 Asystem Radical Relief Gel Roll-on 300mg Cbd
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What is NDC 52261-4901?
What are the uses for Asystem Radical Relief Gel Roll-on 300mg Cbd?
Which are Asystem Radical Relief Gel Roll-on 300mg Cbd UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Asystem Radical Relief Gel Roll-on 300mg Cbd 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)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- MARITIME PINE (UNII: 50JZ5Z98QY)
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
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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".