Label: IT COSMETICS YOUR SKIN BUT BETTER CC PLUS NUDE GLOW COLOR CORRECTING MEDIUM COVERAGE SKIN TINT PLUS BRIGHTENING GLOW SERUM PLUS BROAD SPECTRUM SPF 40 SUNSCREEN- homosalate, octisalate and octocrylene liquid

  • NDC Code(s): 49967-964-01
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 28, 2024

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  • Active ingredients

    Homosalate 7.3%

    Octisalate 5%

    Octocrylene 6%

  • 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 skin aging caused by the sun
  • Warnings

    For external use only

  • Do not use

    on damaged or broken skin

  • When using this product 

    keep our of eyes. Rinse with water to remove

  • Stop use and ask a doctor if

    rash occurs

  • Keep out of reach of children.

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

  • Directions

    For sunscreen use:

    • apply liberally 15 minutes before sun exposure
    • reapply at least every 2 hours 
    • use a water resistant susncreen if swiming or sweating
    • 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 with a Broad Spectrum SPF value of 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
    • children under 6 months of age:

    Ask a doctor

  • Other information

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

    water, glycerin, caprylyl methicone, dimethicone, butyloctyl salicylate, cetyl PEG/PPG-10 dimethicone, niacinamide, propanediol, dimethicone/PEG-10/15 crosspolymer, synthetic fluorphlogopite, phenoxyethanol, sodium chloride
    trimethylsiloxysilicate, disteardimonium hectorite, disodium stearoyl glutamate, fragrance, chlorphenesin, caprylyl glycol, silica silylate, trisodium ethylenediamine disuccinate, limonene, simethicone, maltodextrin, aluminum hydroxide, adenosine, dipropylene glycol, sodium hyaluronate, citral, citric acid, linalool, sodium citrate, camellia sinensis leaf extract, tocopherol, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate; may contain: titanium dioxide, iron oxides

  • Questions or comments?

    Call 800-620-3950

  • PRINCIPAL DISPLAY PANEL

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  • PRINCIPAL DISPLAY PANEL

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  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    IT COSMETICS YOUR SKIN BUT BETTER CC PLUS NUDE GLOW COLOR CORRECTING MEDIUM COVERAGE SKIN TINT PLUS BRIGHTENING GLOW SERUM PLUS BROAD SPECTRUM SPF 40 SUNSCREEN 
    homosalate, octisalate and octocrylene liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-964
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE73 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE60 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    ADENOSINE (UNII: K72T3FS567)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    CITRAL (UNII: T7EU0O9VPP)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-964-011 in 1 CARTON08/01/2024
    132 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/01/2024
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    Beauty Manufacturing Solutions Corp.783200723manufacture(49967-964)
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