Label: COVERGIRL OUTLAST EXTREME WEAR 3-IN-1 FOUNDATION 24 HR FULL COVERAGE SPF 18 OCTINOXATE SUNSCREEN LIQUID FOUNDATION- octinoxate emulsion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2024

If you are a consumer or patient please visit this version.

  • Active Ingredients

    Octinoxate 3.0%

  • Purpose

    Sunscreen

  • Uses

    • helps prevent sunburn
    • if used as directed with other sun protection measures

    (see Directions), decreases the risk of skin cancer and early aging caused by the sun.

  • Warnings

    Skin Cancer/Skin Aging Alert; ;Spending time inthesunincreasesyourriskofskincancerand earlyskinaging.Thisproducthasbeenshown only to help prevent sunburn, not skin cancer or early skin aging.

    For external use only.

  • Do not use

    • on damaged or broken skin.
  • When using this product

    • keep out of eyes. Rinse with water to remove.
  • Stop use and ask doctor if

    • rash occurs.
  • Keep out of reach of children.

    If swollowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • apply liberally 15 minutes before sun exposure
    • useawaterresistantsunscreenif swimming or sweating
    • reapply at least every 2 hours
    • children under 6 months of age: Ask a doctor
    • Sun Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen witha Broad SpectrumSPF valueof 15 or higher and other sun protection measures including:
    • limit time in the sun,especially from 10 a.m.-2 p.m.
    • wear long-sleeved shirts, pants, hats, and sunglasses.
  • Other information

    • protect the product in this container from excessive heat and direct sun.
  • Inactive ingredients

    CYCLOPENTASILOXANE, AQUA/WATER/EAU, TALC, BUTYLENE GLYCOL, CETYL PEG/PPG-10/1 DIMETHICONE, ACRYLATES CROSSPOLYMER, TRIMETHYLSILOXYSILICATE, CETEARYL ETHYLHEXANOATE, DIMETHICONE/ VINYL DIMETHICONE CROSSPOLYMER, MAGNESIUM SULFATE, BIS-PEG/PPG-14/ 14 DIMETHICONE, AMMONIUM

    ACRYLATES COPOLYMER, TRIBEHENIN, DISTEARDIMONIUM HECTORITE, LAURETH-7, LECITHIN, TRIETHOXYCAPRYLYLSILANE, PHENOXYETHANOL, TRIHYDROXYSTEARIN, CHLORPHENESIN, PROPYLENE CARBONATE, ALCOHOL DENAT., DIMETHICONOL, XANTHAN GUM, GLYCERIN, DISODIUM EDTA, TOCOPHERYL ACETATE, DISODIUM DECETH-6 SULFOSUCCINATE, LAURETH-30, SODIUM PCA, UREA, SODIUM DEHYDROACETATE, TREHALOSE, HEXYLENE GLYCOL, POLYQUATERNIUM-51, BHT, CAPRYLYL GLYCOL, TRIACETIN, SODIUM HYALURONATE, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE, [MAY CONTAIN/PEUT CONTENIR/+/-: IRON OXIDES (CI 77491, CI 77492, CI 77499), TITANIUM DIOXIDE (CI 77891)].

  • Questions or comments?

    Call 1-800-426-8374

  • Package Label

    Package Label

  • INGREDIENTS AND APPEARANCE
    COVERGIRL OUTLAST EXTREME WEAR 3-IN-1 FOUNDATION 24 HR FULL COVERAGE SPF 18 OCTINOXATE SUNSCREEN LIQUID FOUNDATION 
    octinoxate emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22700-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    (4-NITROPHENYL)UREA (UNII: DY0F0348GL)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)  
    SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
    LAURETH-30 (UNII: W9D845551A)  
    TREHALOSE (UNII: B8WCK70T7I)  
    BHT (UNII: 1P9D0Z171K)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
    SODIUM PCA (UNII: 469OTG57A2)  
    LAURETH-7 (UNII: Z95S6G8201)  
    TALC (UNII: 7SEV7J4R1U)  
    TRIBEHENIN (UNII: 8OC9U7TQZ0)  
    IRON OXIDES (UNII: 1K09F3G675)  
    TRIHYDROXYSTEARIN (UNII: 06YD7896S3)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    MAGNESIUM SULFATE (UNII: DE08037SAB)  
    BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    TRIACETIN (UNII: XHX3C3X673)  
    PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    DISODIUM DECETH-6 SULFOSUCCINATE (UNII: SX9Q9F5YWB)  
    CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:22700-030-011 in 1 CARTON12/01/2021
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/01/2021
    Labeler - Noxell Corporation (003082997)
    Establishment
    NameAddressID/FEIBusiness Operations
    Noxell Corporation003082997manufacture(22700-030)