Label: ARIZONA SUN SPF 45 SURFBLOK SUNSCREEN- sunscreen spray
- NDC Code(s): 61973-112-04
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 21, 2024
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- Drug Facts
- Active Ingredients
- Purpose
- Uses
- Warnings
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Directions
Apply liberally and evenly to the skin 30 minutes before and during sun exposure. Spray into hands and apply to the face. Avoid contact with eyes. 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
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Inactive Ingredients
SD Alcohol 40B, Acrylates/ Octylacrylamide Copolymer, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Polyol Prepolymer 2, Panthenol, Simmondsia Chinensis (Jojoba) Seed Extract, Biotin, Aloe Barbadensis (Aloe Vera) Leaf Juice, Allantoin, 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, Fragrance
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INGREDIENTS AND APPEARANCE
ARIZONA SUN SPF 45 SURFBLOK SUNSCREEN
sunscreen sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) ALOE VERA LEAF (UNII: ZY81Z83H0X) ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) PANTHENOL (UNII: WV9CM0O67Z) BIOTIN (UNII: 6SO6U10H04) ALLANTOIN (UNII: 344S277G0Z) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SAGE (UNII: 065C5D077J) SUNFLOWER SEED (UNII: R9N3379M4Z) MULLEIN LEAF (UNII: 9936O846LI) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) ALCOHOL (UNII: 3K9958V90M) PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E) HOPS (UNII: 01G73H6H83) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-112-04 120 g in 1 BOTTLE; Type 0: Not a Combination Product 02/21/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/21/2024 Labeler - Arizona Sun Products (107220212)