Label: ARIZONA SUN SUNSCREEN WATER RESISTANT SPF 30- sunscreen lotion
- NDC Code(s): 61973-104-08
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 12, 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, C12-15 Alkyl Benzoate, Stearic Acid, Cyclopentasiloxane, Cyclohexasiloxane, Dimethicone, VP/ Eicosene Copolymer, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Polysorbate 60, Simmondsia Chinensis (Jojoba) Seed Oil, Aloe Barbadensis (Aloe Vera) Leaf Juice, 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, Visicum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, Lanolin, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Triethanolamine, Phenoxyethanol
Ethylhexylglycerin, Fragrance.
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ARIZONA SUN SUNSCREEN WATER RESISTANT SPF 30
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-104 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 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 AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) POLYSORBATE 60 (UNII: CAL22UVI4M) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) LANOLIN (UNII: 7EV65EAW6H) CYCLOMETHICONE 7 (UNII: KCK5L8VU47) ALOE VERA LEAF (UNII: ZY81Z83H0X) HOPS (UNII: 01G73H6H83) PHENOXYETHANOL (UNII: HIE492ZZ3T) SAGE (UNII: 065C5D077J) MULLEIN LEAF (UNII: 9936O846LI) SUNFLOWER SEED (UNII: R9N3379M4Z) CYCLOMETHICONE 6 (UNII: XHK3U310BA) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) WATER (UNII: 059QF0KO0R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) DIMETHICONE (UNII: 92RU3N3Y1O) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PEG-100 STEARATE (UNII: YD01N1999R) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-104-08 946 g in 1 BOTTLE; Type 0: Not a Combination Product 02/12/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/12/2024 Labeler - Arizona Sun Products (107220212)