Label: NYX PROFESSIONAL MAKEUP BUTTERMELT GLAZE SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30- homosalate,octisalate and octocrylene cream

  • NDC Code(s): 49967-356-01
  • Packager: L’Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 23, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • 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 out 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:

    • shake well before use
    • apply liberally 15 minutes before sun exposure
    • reapply at least every 2 hours
    • use a water resistant sunscreen if swimming 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:
          o limit time in the sun, especially from 10am - 2pm

          o 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 excessive heat and direct sun
  • Inactive ingredients

    water, glycerin, caprylyl methicone, dimethicone, silica, butyloctyl salicylate, cetyl PEG/PPG-10/1 dimethicone, niacinamide, propanediol, dimethicone/PEG-10/15 crosspolymer, camellia sinensis leaf extract, mangifera indica (mango) seed butter, butyrospermum parkii (shea) butter, simethicone, sodium chloride, sodium citrate, sodium hyaluronate, silica silylate, trimethylsiloxysilicate, aluminum hydroxide, adenosine, disodium stearoyl glutamate, dipropylene glycol, caprylyl glycol, citric acid, trisodium ethylenediamine disuccinate, maltodextrin, synthetic fluorphlogopite, disteardimonium hectorite, tocopherol, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, phenoxyethanol, chlorphenesin, fragrance, limonene; may contain: titanium dioxide, iron oxides

  • Questions or comments?

    1-844-335-3510

    Monday-Friday

    9 a.m.-5 p.m. EST

  • PRINCIPAL DISPLAY PANEL

    image of a label

  • PRINCIPAL DISPLAY PANEL

    image of a label

  • INGREDIENTS AND APPEARANCE
    NYX PROFESSIONAL MAKEUP BUTTERMELT GLAZE SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30 
    homosalate,octisalate and octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-356
    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) (ETHYLHEXYL SALICYLATE - 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 METHICONE (UNII: Q95M2P1KJL)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SILICA (UNII: ETJ7Z6XBU4)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)  
    CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)  
    MANGIFERA INDICA (MANGO) SEED BUTTER (UNII: 4OXD9M35X2)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
    TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    ADENOSINE (UNII: K72T3FS567)  
    DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    IRON OXIDES (UNII: 1K09F3G675)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-356-011 in 1 CARTON01/10/2024
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/10/2024
    Labeler - L’Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    Beauty Manufacturing Solutions Corp.783200723manufacture(49967-356)