Label: ARIZONA SUN SPF 45 SUNSCREEN- sunscreen spray
- NDC Code(s): 61973-108-04
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 20, 2024
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- Drug Facts
- Active Ingredients
- Purpose
- Uses
- Warnings
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Directions
Apply liberally and evenly to the skin 30 minutes before and during sun exposure. Spray into hands and apply to the face. Avoid contact with eyes. Reapply as needed or after towel drying, perspiring, swimming, and vigorous activities. Use on children under six months of age only wih the advise of a physician.
- Other Information
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Inactive Ingredients
SD Alcohol 40B, Acrylates/ Octylacrylamide Copolymer, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Polyol Prepolymer 2, Panthenol, Simmondsia Chinensis (Jojoba) Seed Extract, Biotin, Aloe Barbadensis (Aloe Vera) Leaf Juice, Allantoin, 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, Viscum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, Fragrance
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INGREDIENTS AND APPEARANCE
ARIZONA SUN SPF 45 SUNSCREEN
sunscreen sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-108 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 50 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 100 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) BIOTIN (UNII: 6SO6U10H04) ALOE VERA LEAF (UNII: ZY81Z83H0X) SAGE (UNII: 065C5D077J) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) HOPS (UNII: 01G73H6H83) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SUNFLOWER SEED (UNII: R9N3379M4Z) PANTHENOL (UNII: WV9CM0O67Z) PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E) ALLANTOIN (UNII: 344S277G0Z) MULLEIN LEAF (UNII: 9936O846LI) ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-108-04 120 g in 1 BOTTLE; Type 0: Not a Combination Product 02/20/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/20/2024 Labeler - Arizona Sun Products (107220212)