Label: ETHYLHEXYL METHOXYCINNAMATE CREAM- detoxifying day cream regular cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 13, 2022

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  • INACTIVE INGREDIENT

    Aqua [water], methyl glucose sesquistearate, butylene glycol, glycerin, caprylic/capric triglyceride, propylheptyl, caprylate, glyceryl stearate, cetearyl alcohol, pentylene glycol, silica, ethylhexyl triazone, diethylamino hydroxybenzoyl hexyl benzoate, propanediol, hydrogenated, polyisobutene, leontopodium alpinum flower/leaf extract, sodium hyaluronate,allantoin, bisabolol, thermus thermophillus ferment, camellia japonica flower extract, glyceryl caprylate, saccharide isomerate, polyisobutene, sodium acrylate/sodium, acryloyldimethyl taurate copolymer, caprylyl/capryl glucoside, sodium stearoyl, lactylate, sorbitan oleate, lecithin, ascorbyl palmitate, BHT, tocopherol, tetrasodium, glutamate diacetate, citric acid, sodium citrate, sodium hydroxide, phenoxyethanol, sodium benzoate, potassium sorbate

  • Directions

    Directions: Every morning, after cleansing evenly spread a small amount of cream over your face, neck and the area above your neckline and gently rub it in.

    Avoid the skin around your eyes.

  • PRINCIPAL DISPLAY PANEL

    ETHYLHEXYL METHOXYCINNAMATE Cream for UV and IR Protection

    Day care cream providing UV and IR protection for oily and combination skin.High-alpine edelweiss combats premature ageing and aggressive environmental influences, while a special active substance with a detoxifying effect purifies the skin and hyaluronic acid and PentavitinTM* smoothe it.

    Outside Packaging

  • INGREDIENTS AND APPEARANCE
    ETHYLHEXYL METHOXYCINNAMATE CREAM 
    detoxifying day cream regular cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70493-520
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE2 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    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)  
    PEG-120 GLYCERYL STEARATE (UNII: 6941286E4I)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    LEONTOPODIUM ALPINUM FLOWERING TOP (UNII: QQC1AK06RK)  
    ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70493-520-021 in 1 BOX02/01/2016
    1NDC:70493-520-0150 mL in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35202/01/2016
    Labeler - inspira: cosmeticsGmbH (329455898)
    Registrant - inspira: cosmeticsGmbH (329455898)
    Establishment
    NameAddressID/FEIBusiness Operations
    inspira: cosmetics GmbH329455898manufacture(70493-520)