Label: ARIZONA SUN KIDS SUNSCREEN SPF 30- sunscreen lotion
- NDC Code(s): 61973-103-04
- Packager: Arizona Sun Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 9, 2024
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Inactive Ingredients
Water, C12-15 Alkyl Benzoate, Cyclopentasiloxane, Stearic Acid, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Glycerin, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Biotin, 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, Viscum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Cetyl Alcohol, Stearyl Alcohol, Carbomer, Sodium PCA, Disodium EDTA,Emulsifying Wax NF, Lanolin, Polysorbate 60, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance.
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INGREDIENTS AND APPEARANCE
ARIZONA SUN KIDS SUNSCREEN SPF 30
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61973-103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 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 OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) SAGE (UNII: 065C5D077J) SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR) PEG-100 STEARATE (UNII: YD01N1999R) CYCLOMETHICONE 7 (UNII: KCK5L8VU47) STEARIC ACID (UNII: 4ELV7Z65AP) DIMETHICONE (UNII: 92RU3N3Y1O) MULLEIN LEAF (UNII: 9936O846LI) LUPINUS LUTEUS SEED (UNII: 39QC7B2817) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) SUNFLOWER SEED (UNII: R9N3379M4Z) HOPS (UNII: 01G73H6H83) ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) VISCUM ALBUM FRUIT (UNII: P83EQ521R3) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) GLYCERIN (UNII: PDC6A3C0OX) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETYL ALCOHOL (UNII: 936JST6JCN) TROLAMINE (UNII: 9O3K93S3TK) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) BIOTIN (UNII: 6SO6U10H04) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) LANOLIN (UNII: 7EV65EAW6H) POLYSORBATE 60 (UNII: CAL22UVI4M) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61973-103-04 0.12 g in 1 BOTTLE; Type 0: Not a Combination Product 02/09/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/09/2024 Labeler - Arizona Sun Products (107220212)
