NDC 58133-100 Real Time Pain Relief Maxx Topical Analgesic
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What is NDC 58133-100?
What are the uses for Real Time Pain Relief Maxx Topical Analgesic?
Which are Real Time Pain Relief Maxx 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 Real Time Pain Relief Maxx 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:
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- HYPERICUM PERFORATUM FLOWER (UNII: A6V4CUE7PV)
- TRIETHANOLAMINE TRIS(DIHYDROGEN PHOSPHATE) (UNII: 36YHT392ID)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CAPSICUM (UNII: 00UK7646FG)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- CENTAUREA CYANUS FLOWER (UNII: QZ239038YC)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CORIANDER OIL (UNII: 7626GC95E5)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EMU OIL (UNII: 344821WD61)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- SORBITOL (UNII: 506T60A25R)
- TILIA X EUROPAEA FLOWER (UNII: NHV2K1OUDH)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- ANTHEMIS ARVENSIS FLOWERING TOP (UNII: 851IP1R9YK)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
What is the NDC to RxNorm Crosswalk for Real Time Pain Relief Maxx Topical Analgesic?
- RxCUI: 1148429 - menthol 1.5 % Topical Lotion
- RxCUI: 1148429 - menthol 15 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".