NDC 70493-560 Ethylhexyl Methoxycinnamate Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70493-560?
Which are Ethylhexyl Methoxycinnamate Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Ethylhexyl Methoxycinnamate 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:
- WATER (UNII: 059QF0KO0R)
- ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
- METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SHEA BUTTER (UNII: K49155WL9Y)
- HYDROGENATED COCO-GLYCERIDES (UNII: XDD37N2GPR)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- LEONTOPODIUM ALPINUM FLOWER (UNII: MWN6IZU3XM)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- LEVOMENOL (UNII: 24WE03BX2T)
- THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)
- HYDROXYPROPYL .BETA.-CYCLODEXTRIN (UNII: 1I96OHX6EK)
- PALMITOYL LYSYLDIOXYMETHIONYLLYSINE (UNII: T7A529FB8O)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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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".