Label: ARIZONA SUN SUNSCREEN SPF 8- sunscreen lotion
- NDC Code(s): 61973-113-04
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 22, 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, Isopropyl Palmitate, Stearic Acid, Glyceryl Stearate, PEG-100 Stearate, Glycerin, Dimethicone, Cetearyl Alcohol, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Polysorbate 60, 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, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance , Titanium Dioxide
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ARIZONA SUN SUNSCREEN SPF 8
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-113 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 10 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 10 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 65 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) SUNFLOWER SEED (UNII: R9N3379M4Z) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SAGE (UNII: 065C5D077J) MULLEIN LEAF (UNII: 9936O846LI) HOPS (UNII: 01G73H6H83) STEARIC ACID (UNII: 4ELV7Z65AP) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) ALOE VERA LEAF (UNII: ZY81Z83H0X) DIMETHICONE (UNII: 92RU3N3Y1O) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERIN (UNII: PDC6A3C0OX) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) POLYSORBATE 60 (UNII: CAL22UVI4M) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) TROLAMINE (UNII: 9O3K93S3TK) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-113-04 120 g in 1 BOTTLE; Type 0: Not a Combination Product 02/02/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/02/2024 Labeler - Arizona Sun Products (107220212)