Label: E.L.F WHOA GLOW BROAD SPECTRUM SPF30 SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene cream

  • NDC Code(s): 76354-443-02, 76354-443-03
  • Packager: e.l.f. Cosmetics, Inc
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 6, 2023

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  • Drug Facts

  • Active Ingredients

    Avobenzone 3.0%

    Homosalate 9.0%

    Octisalate 5.0%

    Octocrylene 7.0%

    Purpose

    Sunscreen

  • Use

    • 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 thsi 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

    • Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours.
    • Use water resistant sunscreen if swimming or sweating.
    • 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 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. Sun Protection Measures:
  • Other Information

    • Protect the product in this container from excessive heat and direct sun.
  • Inactive Ingredients

    Water (Aqua), Glycerin, Polyglyceryl-3 Distearate, Bismuth Oxychloride, Niacinamide, Aluminum Starch Octenylsuccinate, Trehalose, Silica, Panthenol, Sodium Hyaluronate, Squalane, Aloe Barbadensis Leaf Juice, Glyceryl Stearate Citrate, Cetearyl Olivate, Sorbitan Olivate, Stearyl Caprylate, Stearic Acid, Palmitic Acid, Dimethicone, Cetearyl Alcohol, Stearyl Heptanoate, Polyacrylate-13, Polyisobutene, Polysorbate 20, Ethylhexyl Hydroxystearate, Sorbitan Isostearate, Triethoxycaprylylsilane, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Caprylyl Glycol, Ethylhexylglycerin, Potassium Sorbate, Phenoxyethanol, Disodium EDTA, Sodium Benzoate, Citric Acid May Contain: Iron Oxides (CI 77491, CI 77492, CI 77499)

  • Questions or comments?

    1-888-315-9814

  • Package Labeling:

    Outer Package

  • Package Labeling:10ml

    LabelLabel2

  • INGREDIENTS AND APPEARANCE
    E.L.F WHOA GLOW BROAD SPECTRUM SPF30 SUNSCREEN 
    avobenzone, homosalate, octisalate, octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-443
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE90 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)  
    BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    TREHALOSE (UNII: B8WCK70T7I)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SQUALANE (UNII: GW89575KF9)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    STEARYL CAPRYLATE (UNII: 06TS6O9194)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    STEARYL HEPTANOATE (UNII: 2M4UGL1NCN)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76354-443-031 in 1 CARTON09/15/2022
    150 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:76354-443-021 in 1 CARTON09/15/2022
    210 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02009/15/2022
    Labeler - e.l.f. Cosmetics, Inc (093902816)
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