NDC 58133-001 Marathon Pain Relief Topical Analgesic
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What is NDC 58133-001?
Which are Marathon Pain Relief Topical Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Marathon Pain Relief Topical Analgesic 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)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CAPSICUM (UNII: 00UK7646FG)
- CARBOMER 934 (UNII: Z135WT9208)
- CENTAUREA CYANUS FLOWER (UNII: QZ239038YC)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CORIANDER OIL (UNII: 7626GC95E5)
- EMU OIL (UNII: 344821WD61)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- CHAMOMILE (UNII: FGL3685T2X)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- WATER (UNII: 059QF0KO0R)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- SORBITOL (UNII: 506T60A25R)
- EDETATE SODIUM (UNII: MP1J8420LU)
- TILIA X EUROPAEA FLOWER (UNII: NHV2K1OUDH)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Marathon Pain Relief Topical Analgesic?
- RxCUI: 1423826 - menthol 3 % Topical Lotion
- RxCUI: 1423826 - menthol 30 MG/ML Topical Lotion
- RxCUI: 1423831 - Marathon Pain Relief 3 % Topical Lotion
- RxCUI: 1423831 - menthol 30 MG/ML Topical Lotion [Marathon Pain Relief]
- RxCUI: 1423831 - Marathon Pain Relief 30 MG/ML Topical Lotion
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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".