FDA.reportPublic FDA data

32 oz Arizona Sun SPF 30

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 01:53:13

Label at a glance#

ProductArizona Sun Sunscreen SPF 30
Active ingredientAVOBENZONE, OCTISALATE, HOMOSALATE, OXYBENZONE, OCTINOXATE
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. 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

Ethylhexyl Methoxycinnamate (7.50%), Ethylhexyl Salicylate (5.00%), Homosalate (5.00%), Benzophenone-3 (3.00%), Butyl Methoxydibenzoylmethane (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.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop and ask a doctor if

OTC - STOP USE SECTION

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 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

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?

OTC - QUESTIONS SECTION

Call toll free 1-800-442-4786

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

32ozoilfreespf3032ozoilfreespf30

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.arizonasun.com/32ozoilfreespf30.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61973-102-082026-01-29C16284748780-149896155-a4cf-586f-e063-e6dba90add9032 oz Arizona Sun SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61973-102-08Arizona Sun Sunscreen SPF 300.946 g in 1 BOTTLELOTION0.9462

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61973-10261973-102-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
HOPS01G73H6H83IACT
SUNFLOWER SEEDR9N3379M4ZIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
SODIUM PYRROLIDONE CARBOXYLATE469OTG57A2IACT
PEG-100 STEARATEYD01N1999RIACT
SIMMONDSIA CHINENSIS SEEDD24K2Q1F6HIACT
LANOLIN7EV65EAW6HIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
OCTISALATE4X49Y0596WACTIB
HOMOSALATEV06SV4M95SACTIB
CYCLOMETHICONE 7KCK5L8VU47IACT
ROSA CANINA FLOWER81MCR2UQ6QIACT
SAGE065C5D077JIACT
LUPINUS LUTEUS SEED39QC7B2817IACT
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
CETYL ALCOHOL936JST6JCNIACT
DISODIUM EDTA-COPPER6V475AX06UIACT
POLYSORBATE 60CAL22UVI4MIACT
SELENICEREUS GRANDIFLORUS FLOWERII877K4UNRIACT
TROLAMINE9O3K93S3TKIACT
OXYBENZONE95OOS7VE0YACTIB
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
STEARIC ACID4ELV7Z65APIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
ALOE VERA LEAFZY81Z83H0XIACT
VISCUM ALBUM FRUITP83EQ521R3IACT
OCTINOXATE4Y5P7MUD51ACTIB
MULLEIN LEAF9936O846LIIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
BIOTIN6SO6U10H04IACT

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 · 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Arizona Sun Sunscreen SPF 30SUNSCREENArizona Sun Products10e336b3-0aee-cc2f-e063-6394a90a9f912026-04-09WarningsExact identifier
ndc (product): 61973-102
Arizona Sun Sunscreen SPF 30SUNSCREENArizona Sun Products10e4d4b6-23cb-3ee0-e063-6394a90abf9f2026-04-09WarningsExact identifier
ndc (product): 61973-102
Arizona Sun Sunscreen SPF 30SUNSCREENArizona Sun Products10e48195-7bae-2422-e063-6394a90a261c2026-04-09WarningsExact identifier
ndc (product): 61973-102
Arizona Sun Sunscreen SPF 30SUNSCREENArizona Sun Products10e276e4-81f1-9429-e063-6394a90a800d2026-04-09WarningsExact identifier
ndc (package): 61973-102-08
ndc (product): 61973-102
ndc11 (package): 61973010208
spl id: 4f0c8dbb-3b40-522d-e063-6294a90a76ce
spl set id: 10e276e4-81f1-9429-e063-6394a90a800d

Reported adverse events (FAERS/openFDA)#

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