NDC 82075-420 Pain Relief Roll-on
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 82075-420?
What are the uses for Pain Relief Roll-on?
Which are Pain Relief Roll-on UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Pain Relief Roll-on 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:
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- ARNICA MONTANA (UNII: O80TY208ZW)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
- BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)
- PROPANEDIOL (UNII: 5965N8W85T)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYGLYCERYL-6 CAPRYLATE (UNII: DGV8R54VG7)
- POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885)
- POLYGLYCERYL-6 RICINOLEATE (UNII: 8X57R183N7)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATER (UNII: 059QF0KO0R)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- CAPRYLYL GLYCERYL ETHER (UNII: MI97BW74XZ)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
What is the NDC to RxNorm Crosswalk for Pain Relief Roll-on?
- RxCUI: 1600976 - menthol 10 % Topical Solution
- RxCUI: 1600976 - menthol 100 MG/ML Topical Solution
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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".