FDA.reportPublic FDA data

SUNOF Sun Oil SPF 20

Manufacturer
ATAK FARMA KOZMETIK VE KIMYA SANAYI TICARET ANONIM SIRKETI
Effective date
2025-01-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:35:03

Label at a glance#

ProductSUNOF Sun Oil SPF 20
Active ingredientAVOBENZONE, OCTINOXATE
Label structure9 sections

Indications and uses

Helps prevent sunburn If used as directed with other sun proctection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Label contents#

Full prescribing information#

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Paraffinum Liquidum, Daucus Carota

Sativa Seed Oil, Theobroma Cacao Seed Butter, Corylus Avellana

Seed Oil, Parfum, Tocopheryl Acetate, Vitis Vinifera Seed Oil.

Warning

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin.

When using this Product:

Keep out of eyes. Rinse with water to remove.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Octinoxate 7.5%

Other Safety Information

Stop use and ask a doctor if:

Rash occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If Product is swallowed , get medical help or contact a

Poison Control Center right away.

Direction

DOSAGE & ADMINISTRATION SECTION

Apply generously 15 minutes before sun exposure.

Reapply

Protect this Product from excessive heat and direct sun

May stain some fabrics

– After 80 minutes of swimming or sweating.

– Immediately after towel drying.

– At least every 2 hours .

– Children under 6 months : Ask a doctor.

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn

If used as directed with other sun proctection measures (see Directions),

decreases the risk of skin cancer and early skin aging caused by the sun.

Purpose

OTC - PURPOSE SECTION

Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

spf20 Oil.jpgspf20 Oil.jpg

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77418-00477418-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CORYLUS AVELLANA (HAZELNUT) SEED OIL8RQ2839AVGIACT
VITIS VINIFERA (GRAPE) SEED OIL930MLC8XGGIACT
DAUCUS CAROTA SATIVA (CARROT) SEED OIL595AO13F11IACT
AVOBENZONEG63QQF2NOXACTIB
PARAFFINUM LIQUIDUMT5L8T28FGPIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
OCTINOXATE4Y5P7MUD51ACTIB
THEOBROMA CACAO (COCOA) SEED BUTTER512OYT1CRRIACT
PARFUMIDINEA2Q2LHC6MAIACT

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
4fe76a23-a3a6-4e7a-e063-6394a90a7e633c447b68-c0f8-b2d4-e063-6294a90adc362026-04-20WarningsExact identifier
spl set id: 3c447b68-c0f8-b2d4-e063-6294a90adc36

Reported adverse events (FAERS/openFDA)#

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