FDA.reportPublic FDA data

Arizona Sun SPF 45 Surfblok

Manufacturer
Arizona Sun Products
Effective date
2026-04-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:53:16

Label at a glance#

ProductArizona Sun SPF 45 Surfblok Sunscreen
Active ingredientOCTOCRYLENE, AVOBENZONE, OCTINOXATE, OCTISALATE, HOMOSALATE, OXYBENZONE
Label structure9 sections

Indications and uses

Provides high sunburn protection. Higher SPF gives more sunburn protection

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

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

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Provides high sunburn protection. Higher SPF gives more sunburn protection

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash or irritation develops and lasts.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INSTRUCTIONS FOR USE SECTION

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

OTHER SAFETY 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

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

Call toll free 1-800-442-4786

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

surfbloksurfblok

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.allsportsblok.com/surfblok.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61973-112-04Arizona Sun SPF 45 Surfblok Sunscreen120 g in 1 BOTTLESPRAY1202

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61973-11261973-112-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTOCRYLENE5A68WGF6WMACTIB
SIMMONDSIA CHINENSIS SEEDD24K2Q1F6HIACT
ALOE VERA LEAFZY81Z83H0XIACT
ROSA CANINA FLOWER81MCR2UQ6QIACT
SUNFLOWER SEEDR9N3379M4ZIACT
MULLEIN LEAF9936O846LIIACT
LUPINUS LUTEUS SEED39QC7B2817IACT
VISCUM ALBUM FRUITP83EQ521R3IACT
AVOBENZONEG63QQF2NOXACTIB
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW)7LL6SY9YFVIACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
PANTHENOLWV9CM0O67ZIACT
BIOTIN6SO6U10H04IACT
ALLANTOIN344S277G0ZIACT
SELENICEREUS GRANDIFLORUS FLOWERII877K4UNRIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
SAGE065C5D077JIACT
HOMOSALATEV06SV4M95SACTIB
ALCOHOL3K9958V90MIACT
OXYBENZONE95OOS7VE0YACTIB
PPG-12/SMDI COPOLYMER1BK9DDD24EIACT
HOPS01G73H6H83IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Arizona Sun SPF 45 Surfblok SunscreenSUNSCREENArizona Sun Products11e76815-9316-555d-e063-6294a90aeb812026-04-09WarningsExact identifier
ndc (package): 61973-112-04
ndc (product): 61973-112
ndc11 (package): 61973011204
spl id: 4f0c7348-d1c7-1e51-e063-6294a90aa591
spl set id: 11e76815-9316-555d-e063-6294a90aeb81

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.