Label: ARIZONA SUN SUNSCREEN SPF15- sunscreen lotion

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

Drug Label Information

Updated February 7, 2024

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  • Drug Facts

  • Active Ingredients

    Ethylhexyl Methoxycinnamate (7.50%)

    Ethylhexyl Salicylate (3.00%)

    Benzophenone-3 (3.00%)

    Butyl Methoxydibenzoylmethane (Avobenzone) (2.00%)

  • Purpose

    Sunscreen

  • 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 use 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. 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

    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

  • Questions or Comments?

    Call toll free 1-800-442-4786

  • PRINCIPAL DISPLAY PANEL

    1ozspf15

  • INGREDIENTS AND APPEARANCE
    ARIZONA SUN SUNSCREEN SPF15 
    sunscreen lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61973-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE30 mg  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE20 mg  in 1 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61973-101-0130 g in 1 BOTTLE; Type 0: Not a Combination Product02/07/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/07/2024
    Labeler - Arizona Sun Products (107220212)
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