NDC 70493-520 Ethylhexyl Methoxycinnamate Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70493-520?
What are the uses for Ethylhexyl Methoxycinnamate Cream?
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:
- LEVOMENOL (UNII: 24WE03BX2T)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- ALLANTOIN (UNII: 344S277G0Z)
- THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- WATER (UNII: 059QF0KO0R)
- METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- PEG-120 GLYCERYL STEARATE (UNII: 6941286E4I)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- PROPANEDIOL (UNII: 5965N8W85T)
- LEONTOPODIUM ALPINUM FLOWERING TOP (UNII: QQC1AK06RK)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
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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".