Label: E L F CAMO SEMI MATTE CC SPF 30 FAIR 100 W- zinc oxide, titanium dioxide, homosalate, octisalate, octocrylene cream
- NDC Code(s): 76354-530-01
- Packager: e.l.f. Cosmetics, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 6, 2024
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- Drug Facts
- Active ingredients
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- Warning
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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), Dimethicone, Butylene Glycol, Silica, Cetyl PEG/PPG-10/1 Dimethicone, Isononyl Isononanoate, Butyloctyl Salicylate, Polyglyceryl-4 Isostearate, Magnesium Sulfate, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Trehalose, Phenoxyethanol, Hydrated Silica, Disteardimonium Hectorite, Triethoxycaprylylsilane, Hydrogen Dimethicone, Aluminum Hydroxide, Triethyl Citrate, Ethylhexylglycerin, Caprylyl Glycol, Disodium EDTA, Tocopheryl Acetate, Sodium Hyaluronate, Panthenol, Niacinamide, Ascorbyl Palmitate, Canola Oil, Glycerin, Daucus Carota Sativa (Carrot) Seed Oil, 1,2-Hexanediol, Carbomer, Daucus Carota Sativa (Carrot) Root Extract, Polysorbate 20, Helianthus Annuus (Sunflower) Seed Oil, Beta-Carotene, Soluble Collagen, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7 May Contain:Titanium Dioxide (CI 77891), Yellow Iron Oxide (CI 77492), Red Iron Oxide (CI 77491), Black Iron Oxide (CI 77499)
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INGREDIENTS AND APPEARANCE
E L F CAMO SEMI MATTE CC SPF 30 FAIR 100 W
zinc oxide, titanium dioxide, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-530 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 63 mg in 1 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 60 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) TREHALOSE (UNII: B8WCK70T7I) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYDRATED SILICA (UNII: Y6O7T4G8P9) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CAPRYLYL GLYCOL (UNII: 00YIU5438U) EDETATE DISODIUM (UNII: 7FLD91C86K) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PANTHENOL (UNII: WV9CM0O67Z) NIACINAMIDE (UNII: 25X51I8RD4) ASCORBYL PALMITATE (UNII: QN83US2B0N) CANOLA OIL (UNII: 331KBJ17RK) GLYCERIN (UNII: PDC6A3C0OX) CARROT SEED OIL (UNII: 595AO13F11) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CARROT (UNII: L56Z1JK48B) POLYSORBATE 20 (UNII: 7T1F30V5YH) SUNFLOWER OIL (UNII: 3W1JG795YI) BETA CAROTENE (UNII: 01YAE03M7J) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-530-01 1 in 1 CARTON 02/15/2024 1 30 g in 1 TUBE; 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 02/15/2024 Labeler - e.l.f. Cosmetics, Inc. (093902816)
