FDA.reportPublic FDA data

NATURAL SUN AQ SUPER PERFECT 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 22:25:13

Label at a glance#

ProductNATURAL SUN AQ SUPER PERFECT 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, CYCLOMETHICONE, DIPROPYLENE GLYCOL, ETHYLHEXYL METHOXYCINNAMATE, GLYCERIN, CETEARYL ALCOHOL, OCTYLDODECYL NEOPENTANOATE, DICAPRYLYL CARBONATE, POTASSIUM CETYL PHOSPHATE, TRICETEARETH-4 PHOSPHATE, GLYCOL STEARATE, PEG-2 STEARATE, POLYETHYLENE, GLYCERYL STEARATE, PEG-100 STEARATE, STEARIC ACID, POLYGLYCERYL-6 POLYRICINOLEATE, RHEUM UNDULATUM ROOT/STALK/STEM EXTRACT, COPTIS CHINENSIS ROOT EXTRACT, XANTHAN GUM, POLYESTER-5, CAPRYLIC/CAPRIC GLYCERIDES, CAPRYLIC/CAPRIC TRIGLYCERIDE, CRAMBE MARITIMA EXTRACT, CARAPA GUAIANENSIS SEED OIL, ARGANIA SPINOSA KERNEL EXTRACT, HYDROGENATED LECITHIN, SILICA, METHICONE, ACRYLATES/ACRYLAMIDE COPOLYMER, MINERAL OIL, POLYSORBATE 85, ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER, TRIETHANOLAMINE, METHYLPARABEN, DISODIUM EDTA, ETHYLHEXYL SALICYLATE, ISOAMYL-p METHOXYCINNAMATE, 4-METHYLBENZYLIDENE CAMPHOR, BUTYL METHOXYDIBENZOYLMETHANE, FRAGRANCE, ALPHA-ISOMETHYL IONONE, BENTYL BENZOATE, BUTYLPHENY METHYLPROPIONAL, CITRONELLOL, HEXYL CINNAMAL,  LIMONENE, LINALOOL

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
51523-021-012019-10-21C16284748780-1956f9ecf-d2b7-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-021-01NATURAL SUN AQ SUPER PERFECT SUNSPF50 PA50 mL in 1 CARTONCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-021NATURAL SUN AQ SUPER PERFECT SUN SPF50 PA (TITANIUM DIOXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 1 package rows20100715_9842c485-9f9e-463a-b7ae-9c3ede3c84ba.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
51523-02151523-021-01

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
f12a8cdc-3f0c-45b1-bdc1-ba31fbe2e4419842c485-9f9e-463a-b7ae-9c3ede3c84ba2010-07-14Exact identifier
spl id: f12a8cdc-3f0c-45b1-bdc1-ba31fbe2e441
spl set id: 9842c485-9f9e-463a-b7ae-9c3ede3c84ba

Reported adverse events (FAERS/openFDA)#

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