NDC 58133-600 Real Time Pain Relief Cream
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58133-600?
What are the uses for Real Time Pain Relief Cream?
Which are Real Time Pain Relief Cream 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 Cream 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)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CAPSICUM FRUTESCENS WHOLE (UNII: 6XJX33L87P)
- ANTHEMIS ARVENSIS FLOWERING TOP (UNII: 851IP1R9YK)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- CORIANDRUM SATIVUM WHOLE (UNII: 740M8BF6EF)
- WATER (UNII: 059QF0KO0R)
- CALENDULA OFFICINALIS SEED OIL (UNII: 9JS8DS42SV)
- CENTAUREA CYANUS FLOWER (UNII: QZ239038YC)
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- EMU OIL (UNII: 344821WD61)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
- 3,4-METHYLENEDIOXYBENZYL METHYLSULFONE (UNII: 4W601CSX19)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBITOL (UNII: 506T60A25R)
- TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)
- TRIETHANOLAMINE TRIS(DIHYDROGEN PHOSPHATE) (UNII: 36YHT392ID)
What is the NDC to RxNorm Crosswalk for Real Time Pain Relief Cream?
- RxCUI: 240896 - menthol 1.25 % Topical Lotion
- RxCUI: 240896 - menthol 12.5 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".