Label: SEAVENGER OCEAN KISS SUNSCREEN SPF 30- titanium dioxide, zinc oxide cream
- NDC Code(s): 82588-000-01
- Packager: SHOP 709 Corp
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 26, 2023
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Inactive Ingredients:
Water, Caprylyl Methicone, Caprylic/Capric Triglyceride, Butylene Glycol, Ethylhexyl Stearate, Lauryl PEG-10 Tris (Trimethylsiloxy) Silylethyl Dimethicone, Glycerin, Cyclopentasiloxane, C12-15 Alkyl Benzoate, Talc, Isononyl Isononanoate, PEG-10 Dimethicone, Polyhydroxystearic Acid, Magnesium sulfate, Sodium chloride, Alumina, Phenoxyethanol, Chlorphenesin, Phenyl Trimethicone, Stearic Acid, Dimethiconol, Dimethicone, 5 Ethylhexylglycerin, Dimethiconol Crosspolymer, Lauroyl Lysine, Squalane, Maltodextrin, Tocopheryl Acetate, Maltodextrin, Tocopheryl Acetate, Sodium Benzoate, Laminaria Ochroleuca Extract, Marrubium Vulare Extract, Caesalpinia Spinosa Fruit Extract, Helianthus Annuus Sprout Extract
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INGREDIENTS AND APPEARANCE
SEAVENGER OCEAN KISS SUNSCREEN SPF 30
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82588-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 85 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength LAUROYL LYSINE (UNII: 113171Q70B) SQUALANE (UNII: GW89575KF9) MALTODEXTRIN (UNII: 7CVR7L4A2D) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SODIUM BENZOATE (UNII: OJ245FE5EU) LAMINARIA OCHROLEUCA (UNII: 4R2124HE76) HELIANTHUS ANNUUS SPROUT (UNII: 4P26HG1S5W) WATER (UNII: 059QF0KO0R) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) GLYCERIN (UNII: PDC6A3C0OX) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) TALC (UNII: 7SEV7J4R1U) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALUMINUM OXIDE (UNII: LMI26O6933) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) STEARIC ACID (UNII: 4ELV7Z65AP) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82588-000-01 1 in 1 CARTON 04/01/2022 1 118 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 M017 04/01/2022 Labeler - SHOP 709 Corp (025888727)