DR.JART EVERY SUN DAY SUN FLUID

Manufacturer
Have & Be Co., Ltd. | Estee Lauder Companies Inc. | Kolmar Korea Co., Ltd. | Kolmar Korea Co., Ltd
Effective date
2025-01-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:53:42

Label at a glance#

ProductDR.JART EVERY SUN DAY SUN FLUID
Active ingredientOCTINOXATE, OCTOCRYLENE, HOMOSALATE, AVOBENZONE, OCTISALATE
Label structure8 sections

Dosage and administration

■ Apply liberally 15 minutes before sun exposure ■ Reapply at least every two 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, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: * limit time in the sun,...

Storage and handling

■ Protect the product in this container from excessive heat and direct sunlight

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.9%
Homosalate 9.0%
Octinoxate 6.8%
Octisalate 4.5%
Octocrylene 4.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

■ Helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

Stop use

OTC - STOP USE SECTION

and ask a doctor if rash occurs

When using this product

OTC - WHEN USING SECTION

keep out of 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

■ Apply liberally 15 minutes before sun exposure
■ Reapply at least every two 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,
regularly use a sunscreen with a Broad Spectrum
SPF value of 15 or higher and other
sun protection measures including:
* limit time in the sun, especially from 10 am
to 2 pm
* wear long-sleeved shirts, pants, hats, and
sunglasses
■ Children under 6 months of age: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER\AQUA\EAU,
PROPANEDIOL, ALCOHOL
DENAT., BENZOTRIAZOLYL
DODECYL P-CRESOL,
PENTYLENE GLYCOL,
1,2-HEXANEDIOL, SILICA,
DIMETHICONE/VINYL
DIMETHICONE CROSSPOLYMER,
AMMONIUM
ACRYLOYLDIMETHYLTAURATE/
VP COPOLYMER,
STYRENE/ACRYLATES
COPOLYMER, LAVANDULA
ANGUSTIFOLIA (LAVENDER) OIL,
ETHYLHEXYLGLYCERIN,
HYDROXYPROPYL
METHYLCELLULOSE STEAROXY
ETHER, POLYACRYLATE
CROSSPOLYMER-6, BUTYLENE
GLYCOL, LINALOOL, LIMONENE,
BHT, T-BUTYL ALCOHOL,
TOCOPHEROL <ILN50939>

Other information

STORAGE AND HANDLING SECTION

■ Protect the product in this
container from excessive
heat and direct sunlight

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display PanelDr.Jart+

Every Sun Day

Sun Fluid

UVA/UVB Protection

Broad Spectrum

SPF 50+

Sunscreen

100 mL / 3.38fl. oz.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49404-154-012024-01-30C16284748780-11030e365-2e9e-111a-e063-dadaa90a10e2DR.JART EVERY SUN DAY SUN FLUID

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49404-154-01DR.JART EVERY SUN DAY SUN FLUID100 mL in 1 CONTAINERLIQUID1003
49404-154-01DR.JART EVERY SUN DAY SUN FLUID1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49404-154DR.JART EVERY SUN DAY SUN FLUID (HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE) LIQUID [HAVE & BE CO., LTD.]3Current NDC, Legacy NDC, 2 package rows20250126_f06d8f90-f3df-6d76-e053-2a95a90af1f8.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49404-15449404-154-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
DR.JART EVERY SUN DAY SUN FLUIDHOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONEHave & Be Co., Ltd.f06d8f90-f3df-6d76-e053-2a95a90af1f82025-01-24WarningsExact identifier
ndc (package): 49404-154-01
ndc (product): 49404-154
ndc11 (package): 49404015401
spl id: 2c783ebc-cd45-879f-e063-6394a90a8281
spl set id: f06d8f90-f3df-6d76-e053-2a95a90af1f8

Reported adverse events (FAERS/openFDA)#

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