FDA.reportPublic FDA data

1 oz SPF 8

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 Sunscreen SPF 8
Active ingredientAVOBENZONE, OCTISALATE, OCTINOXATE, OXYBENZONE
Label structure9 sections

Indications and uses

Provides minimal 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. Reapply as needed or after towel drying, perspiring, swimming, and vigorous activities. Use on childen under the age of 6 months only wih the advise of a physician.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate (6.50%), Ethylhexyl Salicylate (1.00%), Benzophenone-3 (1.00%), Butyl Methoxydibenzoylmethane (1.00%)

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

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. Reapply as needed or after towel drying, perspiring, swimming, and vigorous activities. Use on childen under the age of 6 months 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

Water, Isopropyl Palmitate, Stearic Acid, Glyceryl Stearate, PEG-100 Stearate, Glycerin, Dimethicone, Cetearyl Alcohol, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Polysorbate 60, Aloe Barbadensis (Aloe Vera) Leaf Juice, Rosa Canina (Rose Hips) Flower 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 (Burdock) Root Extract, Viscum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance , Titanium Dioxide

Questions or Comments?

OTC - QUESTIONS SECTION

Call toll free 1-800-442-4786

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1ozspf81ozspf8

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.arizonasun.com/1ozspf8.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61973-113-01Arizona Sun Sunscreen SPF 830 g in 1 BOTTLELOTION302

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61973-11361973-113-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
ISOPROPYL PALMITATE8CRQ2TH63MIACT
SELENICEREUS GRANDIFLORUS FLOWERII877K4UNRIACT
SUNFLOWER SEEDR9N3379M4ZIACT
OCTISALATE4X49Y0596WACTIB
SIMMONDSIA CHINENSIS SEEDD24K2Q1F6HIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
OCTINOXATE4Y5P7MUD51ACTIB
POLYSORBATE 60CAL22UVI4MIACT
STEARIC ACID4ELV7Z65APIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
PEG-100 STEARATEYD01N1999RIACT
DIMETHICONE92RU3N3Y1OIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
ROSA CANINA FLOWER81MCR2UQ6QIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SAGE065C5D077JIACT
OXYBENZONE95OOS7VE0YACTIB
ALOE VERA LEAFZY81Z83H0XIACT
STEARYL ALCOHOL2KR89I4H1YIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
DISODIUM EDTA-COPPER6V475AX06UIACT
LUPINUS LUTEUS SEED39QC7B2817IACT
HOPS01G73H6H83IACT
TROLAMINE9O3K93S3TKIACT
MULLEIN LEAF9936O846LIIACT
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
VISCUM ALBUM FRUITP83EQ521R3IACT

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 Sunscreen SPF 8SUNSCREENArizona Sun Products11e8b612-29be-47ed-e063-6394a90ab9e72026-04-09WarningsExact identifier
ndc (package): 61973-113-01
ndc (product): 61973-113
ndc11 (package): 61973011301
spl id: 4f0be9a2-5641-baaf-e063-6394a90a0f5b
spl set id: 11e8b612-29be-47ed-e063-6394a90ab9e7

Reported adverse events (FAERS/openFDA)#

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