Label: ARIZONA SUN MOISTURIZER SPF 3- moisturizer lotion
- NDC Code(s): 61973-107-06
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
- Other Information
-
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?
- PRINCIPAL DISPLAY PANEL
-
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 LUPINUS LUTEUS SEED (UNII: 39QC7B2817) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALLANTOIN (UNII: 344S277G0Z) ETHYLHEXYL PALMITATE (UNII: 2865993309) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) ALMOND OIL (UNII: 66YXD4DKO9) MULLEIN LEAF (UNII: 9936O846LI) PANTHENOL (UNII: WV9CM0O67Z) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HOPS (UNII: 01G73H6H83) POLYSORBATE 60 (UNII: CAL22UVI4M) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) SAGE (UNII: 065C5D077J) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) SUNFLOWER SEED (UNII: R9N3379M4Z) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) TROLAMINE (UNII: 9O3K93S3TK) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) CETYL ALCOHOL (UNII: 936JST6JCN) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9) BIOTIN (UNII: 6SO6U10H04) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-107-06 240 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)