Label: ARIZONA SUN MOISTURIZER SPF 3- moisturizer lotion
- NDC Code(s): 61973-107-01
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 16, 2024
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- Active Ingredients
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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.
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INGREDIENTS AND APPEARANCE
ARIZONA SUN MOISTURIZER SPF 3
moisturizer lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 5 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 15 mg in 1 g Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) ETHYLHEXYL PALMITATE (UNII: 2865993309) ALMOND OIL (UNII: 66YXD4DKO9) WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) SAGE (UNII: 065C5D077J) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) TROLAMINE (UNII: 9O3K93S3TK) ALOE VERA LEAF (UNII: ZY81Z83H0X) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) HOPS (UNII: 01G73H6H83) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) BIOTIN (UNII: 6SO6U10H04) PEG-100 STEARATE (UNII: YD01N1999R) PANTHENOL (UNII: WV9CM0O67Z) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) PHENOXYETHANOL (UNII: HIE492ZZ3T) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9) GLYCERIN (UNII: PDC6A3C0OX) MULLEIN LEAF (UNII: 9936O846LI) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) POLYSORBATE 60 (UNII: CAL22UVI4M) STEARIC ACID (UNII: 4ELV7Z65AP) SUNFLOWER SEED (UNII: R9N3379M4Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-107-01 30 g in 1 BOTTLE; Type 0: Not a Combination Product 02/16/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/16/2024 Labeler - Arizona Sun Products (107220212)