Label: SUNBETTER BROAD SPECTRUM SPF 75 SUNSCREEN TONE SMART- zinc oxide, titanium dioxide lotion
- NDC Code(s): 73291-0003-1, 73291-0003-2, 73291-0003-3, 73291-0003-4
- Packager: SKINBETTER SCIENCE LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 31, 2024
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- Drug Facts
- Active Ingredients
- Purpose
- Uses
- Warnings
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Directions
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 the 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.
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Inactive ingredients
1,2-Hexanediol, Acrylates/Dimethicone Copolymer, Allantoin, Alumina, Bis-Vinyl Dimethicone/Dimethicone Copolymer, Bisabolol, Butyloctyl Salicylate, Camellia Oleifera Leaf Extract, Capparis Spinosa Fruit Extract, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cerium Oxide, Cetyl Dimethicone, Dimethicone, Disteardimonium Hectorite, Glycerin, Himanthalia Elongata Extract, Iron Oxides (CI 77491, CI 77492, CI 77499), Mica, Niacinamide, Olea Europaea (Olive) Fruit Extract, Olea Europaea (Olive) Leaf Extract, Opuntia Ficus-Indica Stem Extract, Panthenol, Phenethyl Alcohol, Phenoxyethanol, Phenyl Trimethicone, Plankton Extract, Polyglyceryl-3 Sorbityl Linseedate, Polyglyceryl-4 Oleate, Polygonum Aviculare Extract, Polyhydroxystearic Acid, Polymethyl Methacrylate, Potassium Sorbate, Silica, Sodium Benzoate, Sodium Chloride, Squalane, Stearic Acid, Styrene/Acrylates Copolymer, Tocopheryl Acetate, Triethyl Citrate, Tropolone, Ubiquinone, Water, Zea Mays (Corn) Starch, Zingiber Officinale (Ginger) Root Extract.
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INGREDIENTS AND APPEARANCE
SUNBETTER BROAD SPECTRUM SPF 75 SUNSCREEN TONE SMART
zinc oxide, titanium dioxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73291-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 35 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) GINGER (UNII: C5529G5JPQ) ALLANTOIN (UNII: 344S277G0Z) ALUMINUM OXIDE (UNII: LMI26O6933) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAPRYLYL GLYCOL (UNII: 00YIU5438U) STARCH, CORN (UNII: O8232NY3SJ) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) UBIDECARENONE (UNII: EJ27X76M46) WATER (UNII: 059QF0KO0R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DODECAMETHYLPENTASILOXANE (UNII: 0QDQ2VQ5YJ) OPUNTIA FICUS-INDICA STEM (UNII: MUD8892KHL) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) SQUALANE (UNII: GW89575KF9) STEARIC ACID (UNII: 4ELV7Z65AP) CAPER BERRY (UNII: 7G4C45EE8C) CETYL DIMETHICONE 45 (UNII: IK315POC44) .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) CERIC OXIDE (UNII: 619G5K328Y) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) HIMANTHALIA ELONGATA (UNII: 21RND18XRR) MICA (UNII: V8A1AW0880) NIACINAMIDE (UNII: 25X51I8RD4) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) FERRIC OXIDE RED (UNII: 1K09F3G675) BLACK OLIVE (UNII: 2M6QWV94OC) OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) PANTHENOL (UNII: WV9CM0O67Z) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) POLYGLYCERYL-4 OLEATE (UNII: 15B05TY4GX) POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) TROPOLONE (UNII: 7L6DL16P1T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73291-0003-1 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/01/2021 2 NDC:73291-0003-2 15 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/01/2021 3 NDC:73291-0003-3 1 mL in 1 PACKET; Type 0: Not a Combination Product 02/01/2021 4 NDC:73291-0003-4 237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/01/2021 Labeler - SKINBETTER SCIENCE LLC (049403602)
