NDC 50972-274 Arthritis Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50972 - Newmarket Health Products Llc
- 50972-274 - Arthritis Relief
Product Packages
NDC Code 50972-274-01
Package Description: 57 mL in 1 TUBE
Product Details
What is NDC 50972-274?
What are the uses for Arthritis Relief?
Which are Arthritis Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Arthritis Relief 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- CINNAMON OIL (UNII: E5GY4I6YCZ)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- JOJOBA OIL (UNII: 724GKU717M)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- SQUALANE (UNII: GW89575KF9)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TEA TREE OIL (UNII: VIF565UC2G)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Arthritis Relief?
- RxCUI: 416982 - menthol 1.25 % Topical Cream
- RxCUI: 416982 - menthol 12.5 MG/ML Topical Cream
* 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".