Label: E.L.F. HOLY HYDRATION FACE CREAM SPF 30 SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene cream
- NDC Code(s): 76354-441-50
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- Spending time in the sun increases your risk of sun 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: Sun Protection Measures:
- limit time in the sun, especially from 10 a.m.-2 p.m.
- wear long-sleeved shirt, pants, hats and sunglasses
- children under 6 months of age: Ask doctor.
- Other Information
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Inactive ingredients
Water (Aqua), Glycerin, Polyglyceryl-3 Distearate, Niacinamide, Aluminum Starch Octenylsuccinate, Trehalose, Stearyl Heptanoate, Silica, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Panthenol, Sodium Hyaluronate, Squalane, Butylene Glycol, Stearic Acid, Cetearyl Olivate, Sorbitan Olivate, Cetearyl Alcohol, Glyceryl Stearate Citrate, Dimethicone, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Disodium EDTA, Polyacrylate-13, Polyisobutene, Polysorbate 20, Carbomer, Fragrance(Parfum), Caprylyl Glycol, Phenoxyethanol, Ethylhexylglycerin, Geraniol, Linalool
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INGREDIENTS AND APPEARANCE
E.L.F. HOLY HYDRATION FACE CREAM SPF 30 SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-441 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 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 90 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV) NIACINAMIDE (UNII: 25X51I8RD4) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) TREHALOSE (UNII: B8WCK70T7I) STEARYL HEPTANOATE (UNII: 2M4UGL1NCN) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) PANTHENOL (UNII: WV9CM0O67Z) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SQUALANE (UNII: GW89575KF9) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) STEARIC ACID (UNII: 4ELV7Z65AP) CETEARYL OLIVATE (UNII: 58B69Q84JO) SORBITAN OLIVATE (UNII: MDL271E3GR) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) DIMETHICONE (UNII: 92RU3N3Y1O) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) POLYSORBATE 20 (UNII: 7T1F30V5YH) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GERANIOL (UNII: L837108USY) LINALOOL, (+/-)- (UNII: D81QY6I88E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-441-50 1 in 1 BOX 02/20/2021 1 50 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/20/2021 Labeler - e.l.f. Cosmetics, Inc (093902816)
