NDC 86089-222 Pain Relief Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 86089-222?
What are the uses for Pain Relief Cream?
Which are Pain Relief Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are 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:
- ALLANTOIN (UNII: 344S277G0Z)
- WATER (UNII: 059QF0KO0R)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ASTAXANTHIN (UNII: 8XPW32PR7I)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BISABOLOL OXIDE A (UNII: 16AE65F94Y)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRUS AURANTIIFOLIA FRUIT OIL (UNII: 7937R189CB)
- CURCUMA LONGA LEAF (UNII: H2HC4RY52C)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EMU OIL (UNII: 344821WD61)
- ETHOXYDIGLYCOL BEHENATE (UNII: N76ISC4ZZO)
- GLUCOSAMINE (UNII: N08U5BOQ1K)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TETRASODIUM DIETHYLENETRIAMINEPENTAMETHYLENEPHOSPHONATE (UNII: E6DVO371LC)
- TOCOPHEROL (UNII: R0ZB2556P8)
- VACCINIUM MYRTILLUS LEAF (UNII: Y4U591OU70)
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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".