Label: E L F SUN BOSS GLOSS SPF 25 SUNSCREEN ITS YOUR MAUVE- zinc oxide cream
- NDC Code(s): 76354-129-01
- Packager: e.l.f. Cosmetics, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 8, 2024
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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 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 Board 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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InactiveIngredients
Polyisobutene, Pentaerythrityl Tetraethylhexanoate, Hydrogenated Polysiobutene, C12-15 Alkyl Benzoate, Octyldodecanol, Microcrystalline Wax (Cera Microcristallina), Butyloctyl Salicylate, Tridecyl Trimellitate, Silica Dimethyl Silylate, Oryzanol, Camellia Oleifera Seed Oil, Triethoxycaprylylsilane, Fragrance (Parfum), Ethylhexylglycerin, Polyhydroxystearic Acid, Caprylic/Capric Triglyceride, VP/Hexadecene Copolymer, Tocopheryl Acetate, Ricinus Communis (Castor) Seed Oil, Isostearic Acid, Sodium Hyaluronate, Polyglyceryl-3 Polyricinoleate, Lecithin, Hydrogenated Castor Oil, Tocopherol [+/-]: Iron Oxide (CI 77491), Titanium Dioxide (CI 77891), Iron Oxide (CI 77492), Iron Oxide (CI 77499), Blue 1 Lake (CI 42090), Red 7 Lake (CI 15850)
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INGREDIENTS AND APPEARANCE
E L F SUN BOSS GLOSS SPF 25 SUNSCREEN ITS YOUR MAUVE
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-129 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) OCTYLDODECANOL (UNII: 461N1O614Y) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) TRIDECYL TRIMELLITATE (UNII: FY36J270ES) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) ORYZANOL (UNII: SST9XCL51M) CAMELLIA OIL (UNII: T1PE06G0VE) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CASTOR OIL (UNII: D5340Y2I9G) ISOSTEARIC ACID (UNII: X33R8U0062) HYALURONATE SODIUM (UNII: YSE9PPT4TH) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) TOCOPHEROL (UNII: R0ZB2556P8) FERRIC OXIDE RED (UNII: 1K09F3G675) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 6 (UNII: 481744AI4O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-129-01 1 in 1 CARTON 02/15/2024 1 4 mL 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)
