Drug Facts

Active Ingredients

Homosalate (10.00%), Ethylhexyl Methoxycinnamate (7.50%), Octocrylene (7.00%), Ethylhexyl Salicylate (5.00%), Benzophenone-3 (5.00%), Butyl Methoxydibenzoylmethane (Avobenzone) (3.00%)

Purpose

Sunscreen

Uses

Provides high sunburn protection. Higher SPF gives more sunburn protection

Warnings

For external use only. Do not swallow. Avoid contact with eyes. If contact occurs, rinse eyes thouroughly with water.

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. Spray into hands and apply to the face. Avoid contact with eyes. 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

SD Alcohol 40B, Acrylates/ Octylacrylamide Copolymer, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Polyol Prepolymer 2, Panthenol, Simmondsia Chinensis (Jojoba) Seed Extract, Biotin, Aloe Barbadensis (Aloe Vera) Leaf Juice, Allantoin, 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, Fragrance

Questions or Comments?

Call toll free 1-800-442-4786

surfblok

ARIZONA SUN SPF 45 SURFBLOK SUNSCREEN
sunscreen spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:61973-112
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	70 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
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	50 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV)
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q)
PANTHENOL (UNII: WV9CM0O67Z)
BIOTIN (UNII: 6SO6U10H04)
ALLANTOIN (UNII: 344S277G0Z)
SELENICEREUS GRANDIFLORUS FLOWER (UNII: II877K4UNR)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SAGE (UNII: 065C5D077J)
SUNFLOWER SEED (UNII: R9N3379M4Z)
MULLEIN LEAF (UNII: 9936O846LI)
LUPINUS LUTEUS SEED (UNII: 39QC7B2817)
ALCOHOL (UNII: 3K9958V90M)
PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)
HOPS (UNII: 01G73H6H83)
VISCUM ALBUM FRUIT (UNII: P83EQ521R3)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:61973-112-04	120 g in 1 BOTTLE; Type 0: Not a Combination Product	02/21/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	02/21/2024

Labeler - Arizona Sun Products (107220212)

Arizona Sun SPF 45 Surfblok