Label: ARIZONA SUN SPF 45 SUNSCREEN- sunscreen spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 20, 2024

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  • Drug Facts

  • Active Ingredients

    Homosalate (10.00%), Ethylhexyl Methoxycinnamate (7.50%), Octocrylene (7.00%), Ethylhexyl Salicylate (5.00%), Benzophenone-3 (5.00%), Butyl Methoxydibenzoylmethane (Avobenzone) (3.00%)

  • Purpose

    Sunscreen

  • Uses

    Provides high sunburn protection. Higher SPF gives more sunburn protection

  • Warnings

    For external use only. Do not swallow. Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

    When using this product

    keep out of eyes. Rinse with water to remove.

    Stop and ask a doctor if

    rash or irritation develops and lasts.

    Keep out of the reach of children.

    If swallowed get medical help or contact a poison control center right away.

  • 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

    Sun Alert: Limiting sun exposure, wearing protective clothing, and using suscreen may reduce the risk of skin aging, skin cancer and other harmful effects of the sun.

  • 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

  • Questions or Comments?

    Call toll free 1-800-442-4786

  • PRINCIPAL DISPLAY PANEL

    SPF45spray

  • INGREDIENTS AND APPEARANCE
    ARIZONA SUN SPF 45 SUNSCREEN 
    sunscreen spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61973-108
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE50 mg  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61973-108-04120 g in 1 BOTTLE; Type 0: Not a Combination Product02/20/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/20/2024
    Labeler - Arizona Sun Products (107220212)
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