FDA.reportPublic FDA data

NATURAL SUN ECO Aqua Sunscreen Gel 40 SPF PA+++ 31500176

Manufacturer
THEFACESHOP CO., LTD. | THEFACESHOP NORTH AMERICA, INC.
Effective date
2015-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:09

Label at a glance#

ProductNATURAL SUN ECO Aqua Sunscreen Gel 40 SPF
Active ingredientAVOBENZONE, ENSULIZOLE, OCTINOXATE, OCTISALATE
Label structure10 sections

Indications and uses

Helps prevent sunburn.

Dosage and administration

Apply generously and evenly 15 minutes before sun exposure. Children under 6 months of age: Ask a doctor. Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating. Apply an adequa...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.3%
Ensulizole 3.5%
Octinoxate 6.5%
Octisalate 4.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen
Sunscreen
Sunscreen
Sunscreen

Uses

OTC - PURPOSE SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin

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

Stop use and ask a doctor if rash occurs.

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

Directions

OTC - WHEN USING SECTION

Apply generously and evenly 15 minutes before sun exposure.
Children under 6 months of age: Ask a doctor.
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.
Reapply at least every 2 hours.
Use a water-resistant sunscreen if swimming or sweating.

Apply an adequate amount on the face and neck at the final stage of skincare.

OTHER SAFETY INFORMATION

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

May stain or damage some fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER, CYCLOPENTASILOXANE, ALCOHOL DENAT., ISOAMYL P-METHOXYCINNAMATE, POLYGLYCERYL-6 STEARATE, POLYGLYCERYL-6 BEHENATE, ETHYLHEXYL METHOXYCRYLENE, TROMETHAMINE, DIPROPYLENE GLYCOL, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, SODIUM POLYACRYLATE, PROPANEDIOL, CAPRYLHYDROXAMIC ACID, PANTHENOL, CETEARYL ALCOHOL, POTASSIUM CETYL PHOSPHATE, ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER, SODIUM HYDROXIDE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, XANTHAN GUM, TRISODIUM EDTA, HELIANTHUS ANNUUS (SUNFLOWER) SPROUT EXTRACT, SODIUM BENZOATE, MENTHYL PCA, SODIUM PCA, FRAGRANCE

OTC - QUESTIONS SECTION

Questions or comments? Call 1-866-638-8417

Distributed by:

SPL UNCLASSIFIED SECTION

THEFACESHOP NORTH AMERICA, INC.

Santa Fe Springs, CA 90670

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NATURAL SUN ECO

Aqua Sunscreen Gel

SPF 40 PA+++

[Contains sunflower sprout extract 5000 µg

A sun gel full of moisture that absorbs fast into the skin with coolness.

Applies softly with quick abosorption through skin without stickiness and protects against UV rays.

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-176-042020-01-31C16284748780-19d75b9d0-5380-f424-e053-dadaa90a57ceNATURAL SUN ECO Aqua Sunscreen Gel 40 SPF PA+++ 31500176

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-176-04NATURAL SUN ECOAqua Sunscreen Gel 40 SPF1 in 1 CARTONGEL11
51523-176-04NATURAL SUN ECOAqua Sunscreen Gel 40 SPF50 mL in 1 TUBEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-176NATURAL SUN ECO AQUA SUNSCREEN GEL 40 SPF (AVOBENZONE, ENSULIZOLE, OCTINOXATE AND OCTISALATE GEL) GEL [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20151124_210f121f-506e-229c-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
ENSULIZOLEACTIVE INGREDIENT9YQ9DI1W421
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
ENSULIZOLEACTIVE MOIETY9YQ9DI1W421
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51523-17651523-176-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
ENSULIZOLE9YQ9DI1W42ACTIB
WATER059QF0KO0RIACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB

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
210f121f-506f-229c-e054-00144ff8d46c210f121f-506e-229c-e054-00144ff8d46c2015-10-01WarningsExact identifier
spl id: 210f121f-506f-229c-e054-00144ff8d46c
spl set id: 210f121f-506e-229c-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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