Label: ARIZONA SUN SUNSCREEN WATER RESISTANT SPF 30- sunscreen lotion
- NDC Code(s): 61973-104-01
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 14, 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SUNFLOWER SEED (UNII: R9N3379M4Z) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) POLYSORBATE 60 (UNII: CAL22UVI4M) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) CYCLOMETHICONE 7 (UNII: KCK5L8VU47) CYCLOMETHICONE 6 (UNII: XHK3U310BA) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) TROLAMINE (UNII: 9O3K93S3TK) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) HOPS (UNII: 01G73H6H83) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) LANOLIN (UNII: 7EV65EAW6H) SAGE (UNII: 065C5D077J) MULLEIN LEAF (UNII: 9936O846LI) PEG-100 STEARATE (UNII: YD01N1999R) ALOE VERA LEAF (UNII: ZY81Z83H0X) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-104-01 30 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)
