Active Ingredient

Manufacturer
THANK YOU FARMER CO., LTD | Kolmar Korea Co., Ltd
Effective date
2026-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:54:38

Label at a glance#

ProductTHANK YOU FARMER Sun Project Water Sun Cream
Active ingredientETHYLHEXYL SALICYLATE, OCTOCRYLENE, AVOBENZONE, HOMOSALATE
Label structure12 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient-AVOBENZONE 2.70%, HOMOSALATE` 13.60%, ETHYLHEXYL SALICYLATE 4.50%, OCTOCRYLENE 9.00%

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Purpose

OTC - PURPOSE SECTION

Purpose-Sunscreen, Uses-Helps prevent sunburn

When using this product,

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 to use for children under 6 months

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

Inactive Ingredients-WATER, BUTYLOCTYL SALICYLATE, PROPANEDIOL, BUTYL METHOXYDIBENZOYLMETHANE, POLYMETHYLSILSESQUIOXANE, C20-22 ALKYL PHOSPHATE, C20-22 ALCOHOLS, 1,2-HEXANEDIOL, PENTYLENE GLYCOL, PANTHENOL, METHYL TRIMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, GLYCERYL STEARATE,

VP/EICOSENE COPOLYMER, TROMETHAMINE, POLYACRYLATE CROSSPOLYMER-6, SILICA, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, BUTYLENE GLYCOL, ETHYLHEXYLGLYCERIN, METHYLPROPANEDIOL, POLYETHER-1, GLUTATHIONE, CERAMIDE NP, SODIUM HYALURONATE, TOCOPHEROL, GLYCINE SOJA (SOYBEAN) SEED EXTRACT, BIOSACCHARIDE GUM-1

Other Safety Information

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

Indications & usage

INDICATIONS & USAGE SECTION

Indications & 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

Package Label Principal Display Panel-50+ SUN PROJECT WATER SUN CREAM Broad Spectrum SPF 50+,All Skin Types, Net Wt. 1.69 fl.oz (50mL), Hydrating formula, Non-Greasy finish, Moisture Barrier Care, THANK YOU FARMER

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70618-080-01THANK YOU FARMER Sun Project Water Sun Cream50 g in 1 TUBECREAM501
70618-080-02THANK YOU FARMER Sun Project Water Sun Cream10 in 1 BOXCREAM101
70618-080-03THANK YOU FARMER Sun Project Water Sun Cream6 in 1 CARTONCREAM61

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70618-08070618-080-01, 70618-080-02, 70618-080-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 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
THANK YOU FARMER Sun Project Water Sun CreamAVOBENZONE, ETHYLHEXYL SALICYLATE, HOMOSALATE, OCTOCRYLENETHANK YOU FARMER CO., LTD5004126b-0a9c-21fb-e063-6294a90a52372026-04-21WarningsExact identifier
ndc (package): 70618-080-02
ndc (package): 70618-080-01
ndc (package): 70618-080-03
ndc (product): 70618-080
ndc11 (package): 70618008001
ndc11 (package): 70618008003
ndc11 (package): 70618008002
spl id: 5004126b-0a9d-21fb-e063-6294a90a5237
spl set id: 5004126b-0a9c-21fb-e063-6294a90a5237

Reported adverse events (FAERS/openFDA)#

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