Juyasuyon SPORT ULTRA SUNSCREEN SPRAY

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd
Effective date
2026-08-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-28 00:02:04

Label at a glance#

ProductJUYASUYON Sport Ultra Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure12 sections

Dosage and administration

Shake well. Hold container 4 to 6 inches from the skin to apply. Spray liberally and spread evenly by hand 15 minutes before sun exposure. Do not apply directly into face. Spray on hands then apply to face. Do not use on windy days. Use in well-ventilated area. Reapply: • after 80 minutes of swimming or sweating • immediately after towel dry • reapply at least every 2 hours • Wear long-sleeved shirts, pants, hats,...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.7%
Homosalate 7.5%
Octisalate 4.8%
Octocrylene 10%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Flammable: Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F. Do not use in the presence of a flame or spark. Keep away from sources of ignition – No smoking. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Do not use on

OTC - DO NOT USE SECTION

damaged or broken skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

When using this product:

OTC - WHEN USING SECTION

Keep away from face to avoid breathing. Keep away from eyes. Rinse with water to remove.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Shake well.
Hold container 4 to 6 inches from the skin to apply.
Spray liberally and spread evenly by hand 15 minutes before sun exposure.
Do not apply directly into face. Spray on hands then apply to face.
Do not use on windy days.
Use in well-ventilated area.
Reapply:
• after 80 minutes of swimming or sweating
• immediately after towel dry
• reapply at least every 2 hours
• Wear long-sleeved shirts, pants, hats, and sunglasses
• Children under 6 months of age: Ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

ALCOHOL, DIISOPROPYL SEBACATE, DICAPRYLYL CARBONATE, WATER, MENTHOLUM

Other information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

May stain some fabrics.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136952243229387GTIN-13: 6952243229387
EAN-13: 6952243229387
GTIN storage (14 digits): 06952243229387
00.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
83566-62283566-622-01

Ingredients#

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

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

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
JUYASUYON Sport Ultra SunscreenAVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENEGuangdong Aimu Biological Technology Co., Ltd59d97ee0-e416-53e7-e063-6294a90a91532026-08-25WarningsExact identifier
ndc (package): 83566-622-01
ndc (product): 83566-622
ndc11 (package): 83566062201
spl id: 59d97ee0-e417-53e7-e063-6294a90a9153
spl set id: 59d97ee0-e416-53e7-e063-6294a90a9153

Reported adverse events (FAERS/openFDA)#

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