FDA.reportPublic FDA data

70618-010_SUN PROJECT SKIN-RELIEF SUN CREAM

Manufacturer
THANK YOU FARMER CO., LTD. | Kolmar Korea Co., Ltd
Effective date
2025-04-28
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:39:26

Label at a glance#

ProductSUN PROJECT SKIN-RELIEF SUNCREAM
Active ingredientDIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, ETHYLHEXYL TRIAZONE, BISOCTRIZOLE, ISCOTRIZINOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE 3%
ETHYLHEXYL TRIAZONE 2.4%
METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL 2%
DIETHYLHEXYL BUTAMIDO TRIAZONE 1.2%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure. Reapply at least every two hours


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 of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglasses

Ask a doctor to use for children under 6 months

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

Stop using and ask a doctor if rash occurs

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

INACTIVE INGREDIENT SECTION

WATER, DIBUTYL ADIPATE, PROPANEDIOL, POLYMETHYLSILSESQUIOXANE, NIACINAMIDE, COCO-CAPRYLATE/CAPRATE, CAPRYLYL METHICONE, GLYCERIN, BUTYLENE GLYCOL, 1,2-HEXANEDIOL, PENTYLENE GLYCOL, BEHENYL ALCOHOL, POLY C10-30 ALKYL ACRYLATE, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, DECYL GLUCOSIDE, TROMETHAMINE, CARBOMER, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, SODIUM STEAROYL GLUTAMATE, POLYACRYLATE CROSSPOLYMER-6, ETHYLHEXYLGLYCERIN, ADENOSINE, XANTHAN GUM, CENTELLA ASIATICA EXTRACT, T-BUTYL ALCOHOL, TOCOPHEROL, SALVIA HISPANICA SEED EXTRACT, SOLANUM MELONGENA (EGGPLANT) FRUIT EXTRACT, ANASTATICA HIEROCHUNTICA EXTRACT, LONICERA JAPONICA (HONEYSUCKLE) FLOWER EXTRACT, GARDENIA JASMINOIDES FRUIT EXTRACT, FORSYTHIA SUSPENSA FRUIT EXTRACT, ANGELICA GIGAS ROOT EXTRACT, CNIDIUM OFFICINALE ROOT EXTRACT, COPTIS JAPONICA ROOT EXTRACT, GLYCYRRHIZA URALENSIS (LICORICE) ROOT EXTRACT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70618-010-022024-03-26C16284748780-11030e365-621f-111a-e063-dadaa90a10e270618-010_SUN PROJECT SKIN-RELIEF SUN CREAM
70618-010-022024-01-30C16284748780-11030e365-621f-111a-e063-dadaa90a10e270618-010_SUN PROJECT SKIN-RELIEF SUN CREAM

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70618-010SUN PROJECT SKIN-RELIEF SUNCREAM (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, ETHYLHEXYL TRIAZONE, METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL, DIETHYLHEXYL BUTAMIDO TRIAZONE) CREAM [THANK YOU FARMER CO., LTD.]5Legacy NDC20250429_78802cd7-f3c1-4b3c-92ca-ad93e7f788a4.zip

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70618-01070618-010-01, 70618-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
DIBUTYL ADIPATEF4K100DXP3IACT
PROPANEDIOL5965N8W85TIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
NIACINAMIDE25X51I8RD4IACT
COCOYL CAPRYLOCAPRATE8D9H4QU99HIACT
GLYCERINPDC6A3C0OXIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
PENTYLENE GLYCOL50C1307PZGIACT
BEHENYL ACRYLATE POLYMERD64PM5UT4UIACT
POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATEW19EIO0DBEIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
TROMETHAMINE023C2WHX2VIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)Q7UI015FF9IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ADENOSINEK72T3FS567IACT
XANTHAN GUMTTV12P4NEEIACT
CENTELLA ASIATICA TRITERPENOIDS4YS74Q4G4JIACT
TERT-BUTYL ALCOHOLMD83SFE959IACT
TOCOPHEROLR0ZB2556P8IACT
CHIA SEEDNU0OLX06F8IACT
EGGPLANTW5K7RAS4VKIACT
ANASTATICA HIEROCHUNTICA WHOLESU125S6473IACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
GARDENIA JASMINOIDES FRUIT7CTH8MD549IACT
FORSYTHIA SUSPENSA FRUITP4793M1ES5IACT
ANGELICA GIGAS ROOT32766B2FHXIACT
CNIDIUM OFFICINALE ROOT8S3OZD358JIACT
COPTIS JAPONICA ROOTJH0SWT16D1IACT
GLYCYRRHIZA URALENSIS ROOT42B5YD8F0KIACT
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20ACTIB
ETHYLHEXYL TRIAZONEXQN8R9SAK4ACTIB
BISOCTRIZOLE8NT850T0YSACTIB
ISCOTRIZINOL2UTZ0QC864ACTIB

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
3b4342bd-a454-4314-e063-6294a90aa27878802cd7-f3c1-4b3c-92ca-ad93e7f788a42025-07-31WarningsExact identifier
spl set id: 78802cd7-f3c1-4b3c-92ca-ad93e7f788a4

Reported adverse events (FAERS/openFDA)#

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