NDC 58133-451 Trurelief Rubiton Rub It Where It Hurts
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58133-451?
What are the uses for Trurelief Rubiton Rub It Where It Hurts?
Which are Trurelief Rubiton Rub It Where It Hurts UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Trurelief Rubiton Rub It Where It Hurts 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:
- CAPSICUM (UNII: 00UK7646FG)
- EMU OIL (UNII: 344821WD61)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CORIANDER OIL (UNII: 7626GC95E5)
- TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)
- DEHYDRATED ALCOHOL (UNII: 3K9958V90M)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- CENTAUREA CYANUS FLOWER (UNII: QZ239038YC)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHAMOMILE (UNII: FGL3685T2X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- WATER (UNII: 059QF0KO0R)
- TROLAMINE (UNII: 9O3K93S3TK)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Trurelief Rubiton Rub It Where It Hurts?
- RxCUI: 1442261 - menthol 3 % Topical Cream
- RxCUI: 1442261 - menthol 30 MG/ML Topical Cream
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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".