Label: ARIZONA SUN SUNSCREEN SPF15- sunscreen lotion
- NDC Code(s): 61973-101-04
- Packager: Arizona Sun
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 5, 2024
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Inactive Ingredients
Water, 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 30 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 20 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 Inactive Ingredients Ingredient Name Strength ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) CETYL ALCOHOL (UNII: 936JST6JCN) HOPS (UNII: 01G73H6H83) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) MULLEIN LEAF (UNII: 9936O846LI) SUNFLOWER SEED (UNII: R9N3379M4Z) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) STEARIC ACID (UNII: 4ELV7Z65AP) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) POLYSORBATE 60 (UNII: CAL22UVI4M) PEG-100 STEARATE (UNII: YD01N1999R) ALOE VERA LEAF (UNII: ZY81Z83H0X) SAGE (UNII: 065C5D077J) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIMETHICONE (UNII: 92RU3N3Y1O) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) TROLAMINE (UNII: 9O3K93S3TK) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-101-04 120 g in 1 BOTTLE; Type 0: Not a Combination Product 02/05/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/05/2024 Labeler - Arizona Sun (107220212)