ARIZONA SUN KIDS SUNSCREEN SPF 30- sunscreen lotion

Arizona Sun Kids Sunscreen SPF 30 by

Drug Labeling and Warnings

Arizona Sun Kids Sunscreen SPF 30 by is a Otc medication manufactured, distributed, or labeled by Arizona Sun Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Ethylhexyl Methoxycinnamate (7.50%), Ethylhexyl Salicylate (5.00%), Homosalate (5.00%), Benzophenone-3 (3.00%), Butyl Methoxydibenzoylmethane (3.00%)

Purpose

Sunscreen

Uses

Provides high sunburn protection. Higher SPF gives more sunburn protection.

Warnings

For external use only

When using this product

keep out of eyes. Rinse with water to remove.

Stop and ask a doctor if

rash or irritation develops and lasts.

Keep out of the reach of children.

If swallowed get medical help or contact a poison control center right away.

Directions

Apply liberally and evenly to the skin 30 minutes before and during sun exposure. 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

Sun Alert: Limiting sun exposure, wearing protective clothing, and using suscreen may reduce the risk of skin aging, skin cancer and other harmful effects of the sun.

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.

Questions or Comments?

Call toll free 1-800-442-4786

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARIZONA SUN KIDS SUNSCREEN SPF 30 
sunscreen lotion

Product 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)