Label: E.L.F. ALL SET FOR SUN SPF 45 SUNSCREEN- avobenzone, octisalate, octocrylene spray
- NDC Code(s): 76354-453-01
- Packager: e.l.f. Cosmetics, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 1, 2023
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
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Warnings
For external use only.Do not use on damaged or broken skin.
- When using this product: keep out of eyes. rinse wiht 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.
- Flammable. Do not spray near heat, sparks sources of ignition, or flames.
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Directions
- Apply liberallly 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
Alcohol Denat., Octocrylene, Octisalate, Butyloctyl Salicylate, Isododecane, Diisooctyl Succinate, Avobenzone, Diheptyl Succinate, Silica Caprylyl Silylate, Dicaprylyl Carbonate, Helianthus Annuus (Sunflower) Seed Oil, Citrullus Lanatus (Watermelon) Fruit Extract, Opuntia Ficus-Indica Seed Oil, Bisabolol, PVP, Capryloyl Glycerin/Sebacic Acid Copolymer, Ethyl Ferulate, Tocopherol, Beta-Sitosterol, Squalene, Nylon-12, Lauroyl Lysine
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- Package Label
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INGREDIENTS AND APPEARANCE
E.L.F. ALL SET FOR SUN SPF 45 SUNSCREEN
avobenzone, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-453 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 49 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 95 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 29 mg in 1 mL Inactive Ingredients Ingredient Name Strength DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) BETA-SITOSTEROL (UNII: S347WMO6M4) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) TOCOPHEROL (UNII: R0ZB2556P8) CITRULLUS LANATUS (WATERMELON) FRUIT EXTRACT (UNII: 231473QB6R) NYLON-12 (UNII: 446U8J075B) OPUNTIA FICUS-INDICA SEED OIL (UNII: 1XGW49AK2J) ISODODECANE (UNII: A8289P68Y2) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) LAUROYL LYSINE (UNII: 113171Q70B) BISABOLOL (UNII: 24WE03BX2T) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) DIHEPTYL SUCCINATE (UNII: 057N7SS26Y) DIISOOCTYL SEBACATE (UNII: ZD1TEK0P5Y) ALCOHOL (UNII: 3K9958V90M) SQUALENE (UNII: 7QWM220FJH) PVP (UNII: FZ989GH94E) HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI) ETHYL FERULATE (UNII: 5B8915UELW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-453-01 1 in 1 BOX 09/01/2023 1 60 mL in 1 BOTTLE, SPRAY; 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 09/01/2023 Labeler - e.l.f. Cosmetics, Inc. (093902816)
