Label: ARIZONA SUN SUNSCREEN WATER RESISTANT SPF 30- sunscreen lotion
- NDC Code(s): 61973-104-04
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 13, 2024
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- Active Ingredients
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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 WATER RESISTANT SPF 30
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-104 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 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 OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ALOE VERA LEAF (UNII: ZY81Z83H0X) SAGE (UNII: 065C5D077J) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) TROLAMINE (UNII: 9O3K93S3TK) SUNFLOWER SEED (UNII: R9N3379M4Z) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) CYCLOMETHICONE 7 (UNII: KCK5L8VU47) MULLEIN LEAF (UNII: 9936O846LI) HOPS (UNII: 01G73H6H83) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CYCLOMETHICONE 6 (UNII: XHK3U310BA) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) WATER (UNII: 059QF0KO0R) LANOLIN (UNII: 7EV65EAW6H) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) PHENOXYETHANOL (UNII: HIE492ZZ3T) PEG-100 STEARATE (UNII: YD01N1999R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POLYSORBATE 60 (UNII: CAL22UVI4M) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-104-04 120 g in 1 BOTTLE; Type 0: Not a Combination Product 02/13/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/13/2024 Labeler - Arizona Sun Products (107220212)