FDA.reportPublic FDA data

Sun Project Moisture

Manufacturer
THANK YOU FARMER CO., LTD | Kolmar Korea Co., Ltd
Effective date
2026-01-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:32:52

Label at a glance#

ProductSun Project Moisture
Active ingredientOCTISALATE, OCTINOXATE, OCTOCRYLENE, AVOBENZONE, HOMOSALATE
Label structure12 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

​Active Ingredient:HOMOSALATE 9%, ETHYLHEXYL METHOXYCINNAMATE 6.8%, ETHYLHEXYL SALICYLATE 4.5%, OCTOCRYLENE 4%, BUTYL METHOXYDIBENZOYLMETHANE 2.7%

Purpose

OTC - PURPOSE SECTION

Purpose-Sunscreen, Uses-Helps prevent sunburn

When using

OTC - WHEN USING SECTION

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

Keep Out Of Reach of Children

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

Ask a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor to use for children under 6 months

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged skin, on broken skin

Warning

WARNINGS SECTION

Warning-For external use only

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER, BUTYLOCTYL SALICYLATE, POLYMETHYLSILSESQUIOXANE, NIACINAMIDE, BUTYLENE GLYCOL, ACRYLATES COPOLYMER, C20-22 ALKYL PHOSPHATE, C20-22 ALCOHOLS, GLYCERIN, 1,2-HEXANEDIOL, CAPRYLYL METHICONE, PENTYLENE GLYCOL,CETYL ALCOHOL, POLY C10-30 ALKYL ACRYLATE, TROMETHAMINE, GLYCERYL STEARATE, SILICA, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, DIMETHICONOL, TRISILOXANE, POLYACRYLATE CROSSPOLYMER-6, SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER,POLYISOBUTENE, ETHYLHEXYLGLYCERIN, ADENOSINE, XANTHAN GUM, CAPRYLYL/CAPRYL GLUCOSIDE, SORBITAN OLEATE, T-BUTYL ALCOHOL, PANTHENOL, TOCOPHEROL, CAPRYLIC/CAPRIC TRIGLYCERIDE, POLYGLYCERYL-10 DIISOSTEARATE, HYDROGENATED LECITHIN
,MENADIONE

Other Safety Information

Other Safety Information-Protect the product in this container from excessive heat and direct sun

Incations & usage

INDICATIONS & USAGE SECTION

Incations & usage-Helps prevent sunburn

Dosage & administration

DOSAGE & ADMINISTRATION SECTION

Dosage & administration -Apply liberally 15 minutes before sun exposure. Reapply at least every two hours

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label Principal Display Panel-Thank you Farmer, SPF40 Broad Spectrum, Sun Project Moisture Sun Creaml Sinscren, SPF40 Broad Spectrum, 1.69 FL.OZ/50ml

mm

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70618-040-01Sun Project Moisture50 mL in 1 TUBECREAM503
70618-040-02Sun Project Moisture60 in 1 CARTONCREAM603

Products#

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

DailyMed product names page 1 of 2 · 42 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70618-04070618-040-01, 70618-040-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 40 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
WATER059QF0KO0RIACT
OCTISALATE4X49Y0596WACTIB
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERINPDC6A3C0OXIACT
PENTYLENE GLYCOL50C1307PZGIACT
OCTINOXATE4Y5P7MUD51ACTIB
1,2-HEXANEDIOLTR046Y3K1GIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
C20-22 ALCOHOLSO4M0347C6AIACT
CETYL ALCOHOL936JST6JCNIACT
DIMETHICONOL (100000 CST)OSA9UP217SIACT
TRISILOXANE9G1ZW13R0GIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATEKBC00G95HIIACT
HYDROGENATED POLYISOBUTENE (1300 MW)7D1YQ9Y5EZIACT
ADENOSINEK72T3FS567IACT
TOCOPHEROLR0ZB2556P8IACT
OCTOCRYLENE5A68WGF6WMACTIB
TROMETHAMINE023C2WHX2VIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
NIACINAMIDE25X51I8RD4IACT
AVOBENZONEG63QQF2NOXACTIB
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
CAPRYLYL/CAPRYL OLIGOGLUCOSIDEE00JL9G9K0IACT
TERT-BUTYL ALCOHOLMD83SFE959IACT
HOMOSALATEV06SV4M95SACTIB
MENADIONE723JX6CXY5IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT
XANTHAN GUMTTV12P4NEEIACT
C20-22 ALKYL PHOSPHATEL4VKP0Y7RPIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
SORBITAN OLEATE DECYLGLUCOSIDE CROSSPOLYMERXF9DUA7ABUIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
POLYGLYCERYL-10 ISOSTEARATEZLW9022RH1IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PANTHENOLWV9CM0O67ZIACT
BEHENYL ACRYLATE POLYMERD64PM5UT4UIACT

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
Sun Project MoistureHOMOSALATE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE, OCTOCRYLENE, BUTYL METHOXYDIBENZOYLMETHANETHANK YOU FARMER CO., LTD20a83f02-d851-4aac-e063-6394a90ae1a62026-01-13WarningsExact identifier
ndc (package): 70618-040-02
ndc (package): 70618-040-01
ndc (product): 70618-040
ndc11 (package): 70618004001
ndc11 (package): 70618004002
spl id: 485049b1-9fd6-c1f2-e063-6394a90aaf5d
spl set id: 20a83f02-d851-4aac-e063-6394a90ae1a6

Reported adverse events (FAERS/openFDA)#

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