Label: WETSPORTS ARIZONA SUN WATER RESISTANT SPF 30- sunscreen lotion
- NDC Code(s): 61973-105-02
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 14, 2024
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Inactive Ingredients
Water, C12-15 Alkyl Benzoate, Stearic Acid, Cyclopentasiloxane, Cyclohexasiloxane, Dimethicone, VP/ Eicosene Copolymer, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Polysorbate 60, Simmondsia Chinensis (Jojoba) Seed Oil, Aloe Barbadensis (Aloe Vera) Leaf Juice, Rosa Canina Flower (Rose Hips) Extract, Salvia Officinalis (Sage) Leaf Extract, Verbascum Thapsus (Mullein) Extract, Lupinus Luteus Seed (Lupin) Extract, Humulus Lupulus (Hops) Extract, Cereus Grandiflorus (Cactus) Extract, Arctium Lappa Root (Burdock) Extract, Visicum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, Lanolin, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Triethanolamine, Phenoxyethanol
Ethylhexylglycerin, Fragrance.
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INGREDIENTS AND APPEARANCE
WETSPORTS ARIZONA SUN WATER RESISTANT SPF 30
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-105 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) TROLAMINE (UNII: 9O3K93S3TK) POLYSORBATE 60 (UNII: CAL22UVI4M) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) DIMETHICONE (UNII: 92RU3N3Y1O) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) HOPS (UNII: 01G73H6H83) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ALOE VERA LEAF (UNII: ZY81Z83H0X) LANOLIN (UNII: 7EV65EAW6H) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) SAGE (UNII: 065C5D077J) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) CYCLOMETHICONE 7 (UNII: KCK5L8VU47) PEG-100 STEARATE (UNII: YD01N1999R) MULLEIN LEAF (UNII: 9936O846LI) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CYCLOMETHICONE 6 (UNII: XHK3U310BA) WATER (UNII: 059QF0KO0R) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SUNFLOWER SEED (UNII: R9N3379M4Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-105-02 60 g in 1 BOTTLE; Type 0: Not a Combination Product 02/14/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/14/2024 Labeler - Arizona Sun Products (107220212)