FDA.reportPublic FDA data

INNISFREE DAILY UV INVISIBLE BARRIER SUNSCREEN SERUM

Manufacturer
Innisfree Corporation
Effective date
2026-05-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-07-17 21:34:49

Label at a glance#

ProductINNISFREE DAILY UV INVISIBLE BARRIER SUNSCREEN SERUM
Active ingredientHOMOSALATE, AVOBENZONE, OCTISALATE
Label structure10 sections

Indications and uses

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

Dosage and administration

■ Apply liberally 15 minutes be- fore sun exposure. ■ Reapply at least every 2 hours. ■ Use a water-resistant sunscreen if swimming or sweating. ■ Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regul- arly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the s...

Storage and handling

Protect the product in this container from excessive heat and direct sun.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.5%
Homosalate 5.0%
Octisalate 4.5%

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

USES

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

OTC - DO NOT USE SECTION

  • Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

  • When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

■ Apply liberally 15 minutes be- fore sun exposure.
■ Reapply at least every 2 hours.
■ Use a water-resistant sunscreen if swimming or sweating.
■ Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regul- arly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

  • Limit time in the sun, espe- cially from 10 a.m. - 2 p.m.
  • Wear long-sleeved shirts, pa- nts, hats, and sunglasses.

■ Children under 6 months of age: Ask a doctor.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Protect the product in this container from excessive heat and direct sun.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ater / Aqua / Eau, Glycerin, Ethylhexyl Methoxycrylene, Phenyl Trimethicone, Caprylyl Methicone, 1,2-Hexanediol, Behenyl Alcohol, Glyceryl Polymethacrylate, Panthenol, Sodium Polyacryloyl- dimethyl Taurate, Arachidyl Alcohol, Propanediol, Butylene Glycol, Ethylhexylglycerin, Caprylyl Glycol, Polyacrylate Crosspolymer-6, Arachidyl Glucoside, Niacinamide, Tocopherol,

Sodium Metaphosphate, Madecassoside, Sodium Hyaluronate, Hyaluronic Acid, Cetyl-PG Hydroxyethyl Palmitamide, Glyceryl Oleate, Tromethamine, Lecithin, Lauryl Glucoside, Polyglyceryl-6 Laurate, Myristyl Glucoside, Camellia Sinensis Leaf Extract, Camellia Sinensis Flower Extract, Xanthan Gum

Questions?

POSTMARKETING EXPERIENCE SECTION

global@cosrx.co.kr

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncarton

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71220-09171220-091-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPRYLYL GLYCOL00YIU5438UIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
HOMOSALATEV06SV4M95SACTIB
CAPRYLYL METHICONEQ95M2P1KJLIACT
WATER059QF0KO0RIACT
PANTHENOLWV9CM0O67ZIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERYL OLEATE4PC054V79PIACT
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
HYALURONIC ACIDS270N0TRQYIACT
SODIUM HYALURONATEYSE9PPT4THIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
PROPANEDIOL5965N8W85TIACT
NIACINAMIDE25X51I8RD4IACT
TOCOPHEROLR0ZB2556P8IACT
CETYL-PG HYDROXYETHYL PALMITAMIDEISA73Z2140IACT
SODIUM POLYACRYLOYLDIMETHYL TAURATENG5NG5733TIACT
GLYCERINPDC6A3C0OXIACT
BEHENYL ALCOHOL9G1OE216XYIACT
GLYCERYL POLYMETHACRYLATE (300000 MPA.S)2B25A5KAD6IACT
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
MADECASSOSIDECQ2F5O6YIYIACT
XANTHAN GUMTTV12P4NEEIACT
CAMELLIA SINENSIS LEAFW2ZU1RY8B0IACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
TROMETHAMINE023C2WHX2VIACT
POLYGLYCERYL-6 LAURATEQ48X4BL3TVIACT
SODIUM METAPHOSPHATE532IUT7IRVIACT
MYRISTYL GLUCOSIDE6AK28695LFIACT
CAMELLIA SINENSIS FLOWER9I2BJY2J17IACT
POLYACRYLATE CROSSPOLYMER-6Q7UI015FF9IACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT

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
INNISFREE DAILY UV INVISIBLE BARRIER SUNSCREEN SERUMAVOBENZONE, HOMOSALATE, AND OCTISALATEInnisfree Corporation524264b8-d360-1d7b-e063-6394a90ab1152026-05-21WarningsExact identifier
ndc (package): 71220-091-08
ndc (product): 71220-091
ndc11 (package): 71220009108
spl id: 5259c6d3-b804-2c24-e063-6394a90a427a
spl set id: 524264b8-d360-1d7b-e063-6394a90ab115

Reported adverse events (FAERS/openFDA)#

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