ARIZONA SUN KIDS SUNSCREEN SPF 30- sunscreen lotion 
Arizona Sun Products

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4 oz Arizona Sun Kids SPF 30

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

4ozkidsof30

ARIZONA SUN KIDS SUNSCREEN SPF 30 
sunscreen lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61973-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE30 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61973-103-040.12 g in 1 BOTTLE; Type 0: Not a Combination Product02/09/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/09/2024
Labeler - Arizona Sun Products (107220212)

Revised: 2/2024
Document Id: 10f60367-6682-a589-e063-6394a90a6bb8
Set id: 10f60367-6681-a589-e063-6394a90a6bb8
Version: 1
Effective Time: 20240209
 
Arizona Sun Products