Label: ARIZONA SUN MOISTURIZER SPF 3- moisturizer lotion

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

Drug Label Information

Updated February 15, 2024

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  • Drug Facts

  • Active Ingredients

    Ethylhexyl Methoxycinnamate (1.50%), Benzophenone-3 (0.50%)

  • 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 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, Stearic Acid, Glyceryl Stearate, PEG-100 Stearate, Glycerin, C12-15 Alkyl Benzoate, Cetyl Alcohol, Panthenol, Allantoin, Carbomer, Ethylhexyl Palmitate, Tocopheryl Acetate (Vitamin E), Simmondsia Chinensis (Jojoba) Seed Oil, Ethylhexyl Stearate, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Aloe Barbadensis (Aloe Vera) Leaf Juice, Sodium PCA, 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, Biotin, Caprylic/ Capric Triglyceride, Polysorbate 60, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance, Titanium Dioxide.

  • Questions or Comments?

    Call toll free 1-800-442-4786

  • PRINCIPAL DISPLAY PANEL

    32ozmoist

  • INGREDIENTS AND APPEARANCE
    ARIZONA SUN MOISTURIZER SPF 3 
    moisturizer lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61973-107
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE15 mg  in 1 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR)  
    HOPS (UNII: 01G73H6H83)  
    CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SAGE (UNII: 065C5D077J)  
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    LUPINUS LUTEUS SEED (UNII: 39QC7B2817)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    BIOTIN (UNII: 6SO6U10H04)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    MULLEIN LEAF (UNII: 9936O846LI)  
    VISCUM ALBUM FRUIT (UNII: P83EQ521R3)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)  
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
    SUNFLOWER SEED (UNII: R9N3379M4Z)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALLANTOIN (UNII: 344S277G0Z)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61973-107-08960 g in 1 BOTTLE; Type 0: Not a Combination Product02/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/15/2024
    Labeler - Arizona Sun Products (107220212)
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