Label: ARIZONA SUN SUNSCREEN KIDS WATER RESISTANT SPF 30- sunscreen lotion
- NDC Code(s): 61973-106-01
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 15, 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
ARIZONA SUN SUNSCREEN KIDS WATER RESISTANT SPF 30
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-106 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CYCLOMETHICONE 7 (UNII: KCK5L8VU47) CYCLOMETHICONE 6 (UNII: XHK3U310BA) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) MULLEIN LEAF (UNII: 9936O846LI) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) DIMETHICONE (UNII: 92RU3N3Y1O) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) HOPS (UNII: 01G73H6H83) WATER (UNII: 059QF0KO0R) LANOLIN (UNII: 7EV65EAW6H) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) TROLAMINE (UNII: 9O3K93S3TK) PHENOXYETHANOL (UNII: HIE492ZZ3T) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) SUNFLOWER SEED (UNII: R9N3379M4Z) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) PEG-100 STEARATE (UNII: YD01N1999R) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) POLYSORBATE 60 (UNII: CAL22UVI4M) SAGE (UNII: 065C5D077J) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALOE VERA LEAF (UNII: ZY81Z83H0X) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-106-01 30 g in 1 BOTTLE; Type 0: Not a Combination Product 02/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/15/2024 Labeler - Arizona Sun Products (107220212)