Label: ARIZONA SUN SUNSCREEN SPF15- sunscreen lotion
- NDC Code(s): 61973-101-01
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 7, 2024
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Inactive Ingredients
Water (Agua), Stearic Acid, Propylene Glycol, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Cetyl Alcohol, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Aloe Barbadensis (Aloe Vera) Leaf Juice, Rosa Canina (Rose Hips) Flower 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 (Burdock) Root Extract, Viscum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract,
Polysorbate 60, Cetearyl Alcohol, Carbomer, Glycerin, Disodium EDTA, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance
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INGREDIENTS AND APPEARANCE
ARIZONA SUN SUNSCREEN SPF15
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-101 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 30 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 20 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength LUPINUS LUTEUS SEED (UNII: 39QC7B2817) WATER (UNII: 059QF0KO0R) MULLEIN LEAF (UNII: 9936O846LI) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) HOPS (UNII: 01G73H6H83) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PEG-100 STEARATE (UNII: YD01N1999R) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) TROLAMINE (UNII: 9O3K93S3TK) ALOE VERA LEAF (UNII: ZY81Z83H0X) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) SUNFLOWER SEED (UNII: R9N3379M4Z) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIMETHICONE (UNII: 92RU3N3Y1O) SAGE (UNII: 065C5D077J) POLYSORBATE 60 (UNII: CAL22UVI4M) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) STEARIC ACID (UNII: 4ELV7Z65AP) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-101-01 30 g in 1 BOTTLE; Type 0: Not a Combination Product 02/07/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/07/2024 Labeler - Arizona Sun Products (107220212)