NDC 24488-002 Pain Reliefroll On Roll On
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 24488-002?
What are the uses for Pain Reliefroll On Roll On?
Which are Pain Reliefroll On Roll On UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR, (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR, (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Pain Reliefroll On 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:
- WATER (UNII: 059QF0KO0R)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WAX, YELLOW (UNII: 2ZA36H0S2V)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPSAICIN (UNII: S07O44R1ZM)
What is the NDC to RxNorm Crosswalk for Pain Reliefroll On Roll On?
- RxCUI: 1044579 - camphor 4 % / capsaicin 0.03 % / menthol 10 % / methyl salicylate 30 % Topical Solution
- RxCUI: 1044579 - camphor 40 MG/ML / capsaicin 0.3 MG/ML / menthol 100 MG/ML / methyl salicylate 300 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".