NDC 70984-001 Raging Kakapo Pain Relieve
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70984 - Effihealth Llc
- 70984-001 - Raging Kakapo Pain Relieve
Product Packages
NDC Code 70984-001-01
Package Description: 1 JAR in 1 CARTON / 113.4 g in 1 JAR
Product Details
What is NDC 70984-001?
What are the uses for Raging Kakapo Pain Relieve?
Which are Raging Kakapo Pain Relieve UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
Which are Raging Kakapo Pain Relieve 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- EMU OIL (UNII: 344821WD61)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- NIACINAMIDE (UNII: 25X51I8RD4)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- STEARETH-21 (UNII: 53J3F32P58)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ARNICA MONTANA (UNII: O80TY208ZW)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- STEARETH-2 (UNII: V56DFE46J5)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Raging Kakapo Pain Relieve?
- RxCUI: 1986870 - capsaicin 0.025 % / histamine dihydrochloride 0.075 % Topical Cream
- RxCUI: 1986870 - capsaicin 0.25 MG/ML / histamine dihydrochloride 0.75 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".