Label: ARIZONA SUN SUNSCREEN SPF 8- sunscreen lotion

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

Drug Label Information

Updated February 22, 2024

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  • Drug Facts

  • Active Ingredients

    Ethylhexyl Methoxycinnamate (6.50%)

    Ethylhexyl Salicylate (1.00%)

    Benzophenone-3 (1.00%)

    Butyl Methoxydibenzoylmethane (1.00%)

  • Purpose

    Provides Minimal Sunburn Protection

  • Uses

    Provides minimal sunburn protection. Higher SPF gives more sunburn protection.

  • Warnings

    For external use only.

    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. Reapply as needed or after towel drying, perspiring, swimming, and vigorous activities.

  • 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

    Water, Isopropyl Palmitate, Stearic Acid, Glyceryl Stearate, PEG-100 Stearate, Glycerin, Dimethicone, Cetearyl Alcohol, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Polysorbate 60, 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, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance , Titanium Dioxide

  • Questions?

    Call toll free 1-800-442-4786

  • PRINCIPAL DISPLAY PANEL

    4ozspf8

  • INGREDIENTS AND APPEARANCE
    ARIZONA SUN SUNSCREEN SPF 8 
    sunscreen lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61973-113
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE10 mg  in 1 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE10 mg  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE65 mg  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
    SUNFLOWER SEED (UNII: R9N3379M4Z)  
    LUPINUS LUTEUS SEED (UNII: 39QC7B2817)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SAGE (UNII: 065C5D077J)  
    MULLEIN LEAF (UNII: 9936O846LI)  
    HOPS (UNII: 01G73H6H83)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q)  
    SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    VISCUM ALBUM FRUIT (UNII: P83EQ521R3)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61973-113-04120 g in 1 BOTTLE; Type 0: Not a Combination Product02/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/02/2024
    Labeler - Arizona Sun Products (107220212)
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