ARIZONA SUN SUNSCREEN WATER RESISTANT SPF 30- sunscreen lotion

Arizona Sun Sunscreen Water Resistant SPF 30 by

Drug Labeling and Warnings

Arizona Sun Sunscreen Water Resistant 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 highl 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 use 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, 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?

Call toll free 1-800-442-4786

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARIZONA SUN SUNSCREEN WATER RESISTANT SPF 30 
sunscreen lotion

Product 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)