Label: E L F WHOA GLOW BROAD SPECTRUM SPF 30 SUNSCREEN SHEER BRONZE SHIMMER SUNBURST- avobenzone, homosalate, octisalate, octocrylene cream
- NDC Code(s): 76354-451-01
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2024
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- Drug Facts
- Active Ingredients
- Use
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours.
- Use 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: 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
- Other Information
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Inactive Ingredients
Water (Aqua), Glycerin, Polyglyceryl-3 Distearate, Niacinamide, Synthetic Fluorphogopite, Trehalose, Stearyl Heptanoate, Silica, Aloe Barbadensis Leaf Juice, Panthenol, Squalane, Sodium Hyaluronate, Caprylyl Glycol, Ethylhexylglycerin, Cetearyl Alcohol, Palmitic Acid, Cetearyl Olivate, Stearic Acid, Sorbitan Olivate, Polyacrylate-13, Glyceryl Stearate Citrate, Polyisobutene, Dimethicone, Polysorbate 20, Sorbitan Isostearate, Potassium Sorbate, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Mica, Phenoxyethanol, Citric Acid, Disodium EDTA, Sodium Benzoate May Contain:Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77499), Yellow 5 (CI 19140)
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INGREDIENTS AND APPEARANCE
E L F WHOA GLOW BROAD SPECTRUM SPF 30 SUNSCREEN SHEER BRONZE SHIMMER SUNBURST
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-451 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 73 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 40 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 85 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV) NIACINAMIDE (UNII: 25X51I8RD4) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) TREHALOSE (UNII: B8WCK70T7I) STEARYL HEPTANOATE (UNII: 2M4UGL1NCN) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ALOE VERA LEAF (UNII: ZY81Z83H0X) PANTHENOL (UNII: WV9CM0O67Z) SQUALANE (UNII: GW89575KF9) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PALMITIC ACID (UNII: 2V16EO95H1) CETEARYL OLIVATE (UNII: 58B69Q84JO) STEARIC ACID (UNII: 4ELV7Z65AP) SORBITAN OLIVATE (UNII: MDL271E3GR) POLYACRYLATE-13 (UNII: FS2D4T67EA) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O) POLYSORBATE 20 (UNII: 7T1F30V5YH) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) MICA (UNII: V8A1AW0880) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-451-01 50 mL in 1 TUBE; Type 0: Not a Combination Product 07/20/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/20/2024 Labeler - e.l.f. Cosmetics, Inc (093902816)
