NDC 64058-356 Pure Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64058 - Concept Laboratories, Inc.
- 64058-356 - Pure Relief
Product Packages
NDC Code 64058-356-34
Package Description: 113 g in 1 JAR
Product Details
What is NDC 64058-356?
What are the uses for Pure Relief?
Which are Pure Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Pure 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:
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)
- ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- LAURYL LAURATE (UNII: GPW77G0937)
- STARCH, CORN (UNII: O8232NY3SJ)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALFALFA (UNII: DJO934BRBD)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CYMBOPOGON SCHOENANTHUS TOP (UNII: 9SJI1LW39W)
- ROSEMARY (UNII: IJ67X351P9)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- GINKGO (UNII: 19FUJ2C58T)
- FLAX SEED (UNII: 4110YT348C)
- CELOSIA ARGENTEA SEED (UNII: O1H314U8M2)
- ACAI (UNII: 46AM2VJ0AW)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- EMU OIL (UNII: 344821WD61)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Pure Relief?
- RxCUI: 198555 - capsaicin 0.025 % Topical Cream
- RxCUI: 198555 - capsaicin 0.25 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".