FDA.reportPublic FDA data

NATURAL SUN AQ SUPER WHITE SUN

Manufacturer
THEFACESHOP CO., LTD.
Effective date
2010-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:14

Label at a glance#

ProductNATURAL SUN AQ SUPER WHITE SUN SPF50 PA
Active ingredientTITANIUM DIOXIDE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: TITANIUM DIOXIDE

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

WATER, CYCLOPENTASILOXANE, ETHYLHEXYL METHOXYCINNAMATE, SD ALCOHOL 40-B, CYCLOMETHICONE, DICAPRYLYL CARBONATE, OCTYLDODECYL NEOPENTANOATE, SORBITAN STEARATE, SORBITYL LAURATE, DIPROPYLENE, GLYCOL, DIISOPROPYL ADIPATE, POTASSIUM CETYL PHOSPHATE, CETEARYL ALCOHOL, PEG-100 STEARATE,
GLYCERYL STEARATE DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, DIMETHICONE, METHYL METHACRYLATE CROSSPOLYMER, SILICA, METHICONE, RHEUM UNDULATUM ROOT/STALK/STEM EXTRACT, COPTIS CHINENSIS ROOT EXTRACT, GLYCERIN, ARGANIA SPINOSA KERNEL EXTRACT, CRAMBE MARITIMA EXTRACT, CAPRYLIC/CAPRIC TRIGLYCERIDE, MORUS ALBA BARK EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, ALOE FEROX LEAF EXTRACT, ETHYLHEXYL SALICYLATE, ARCTIUM LAPPA ROOT EXTRACT, ARTEMISIA PRINCEPS LEAF EXTRACT, POLYESTER-5, STEARIC ACID, XANTHAN GUM, PINUS STROBUS BARK EXTRACT, BUTYL METHOXYDIBENZOYLMETHANE, HYDROGENATED LECITHIN, POLYGLYCERYL-6 POLYRICINOLEATE, ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER, 4-METHYLBENZYLIDENE CAMPHOR, ISOAMYL P-METHOXYCINNAMATE, CAPRYLIC/CAPRIC GLYCERIDES, DISODIUM EDTA, METHYLPARABEN POTASSIUM HYDROXIDE, FRAGRANCE

DESCRIPTION SECTION

Warnings:
When using this product
Keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if
Rash or irritation develops and lasts.

Directions:
Apply evenly before sun exposure and as needed.
Children under 6months of age; ask a doctor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-022-012019-10-21C16284748780-1956f9ecf-bb23-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-022-01NATURAL SUN AQ SUPER WHITE SUNSPF50 PA50 mL in 1 CARTONCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-022NATURAL SUN AQ SUPER WHITE SUN SPF50 PA (TITANIUM DIOXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 1 package rows20100715_f9e48ab7-6d60-41a0-94c6-f5c25ce971cc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
TITANIUMACTIVE MOIETYD1JT611TNE1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51523-02251523-022-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
4c2ad6f4-78e0-4d04-83d2-67011e511480f9e48ab7-6d60-41a0-94c6-f5c25ce971cc2010-07-14Exact identifier
spl id: 4c2ad6f4-78e0-4d04-83d2-67011e511480
spl set id: f9e48ab7-6d60-41a0-94c6-f5c25ce971cc

Reported adverse events (FAERS/openFDA)#

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