Label: E.L.F SUN BOSS GLOSS SPF 25 SUNSCREEN BLUSH MUCH- zinc oxide cream
- NDC Code(s): 76354-127-01
- 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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- 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 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
Polyisobutene, Pentaerythrityl Tetraethylhexanoate, Hydrogenated Polyisobutene, C12-15 Alkyl Benzoate, Tridecyl Trimellitate, Octyldodecanol, Microcrystalline Wax (Cera Microcristallina), Butyloctyl Salicylate, Oryzanol, Camellia Oleifera Seed Oil, Triethoxycaprylylsilane, Fragrance (Parfume), Ethylhexylglycerin, Polyhydroxystearic Acid, Caprylic/Capric Triglyceride, VP/Hexadecene Copolymer, Tocopheryl Acetate, Ricinus Communis (Castor) Seed Oil, Isostearic Acid, Sodium Hyaluronate, Lecithin, Hydrogenated Castor Oil, Tocopherol (+/-): Iron Oxide (CI 77492), Iron Oxide (CI 77491), Red 6 Lake (CI 15850), Red 7 Lake (CI 15850), Iron Oxide (CI 77499), Titanium Dioxide (CI 77891)
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INGREDIENTS AND APPEARANCE
E.L.F SUN BOSS GLOSS SPF 25 SUNSCREEN BLUSH MUCH
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-127 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) TRIDECYL TRIMELLITATE (UNII: FY36J270ES) OCTYLDODECANOL (UNII: 461N1O614Y) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) 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) TOCOPHEROL (UNII: R0ZB2556P8) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERRIC OXIDE RED (UNII: 1K09F3G675) D&C RED NO. 6 (UNII: 481744AI4O) FERROSOFERRIC OXIDE (UNII: XM0M87F357) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-127-01 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)