FDA.reportPublic FDA data

SUPER ORIGIN COTTON FINISH FOUNDATION

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2014-05-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:39:11

Label at a glance#

ProductSUPER ORIGIN COTTON FINISH FOUNDATION 21 LIGHT BEIGE
Active ingredientTitanium Dioxide, OCTINOXATE, Zinc Oxide
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Titanium Dioxide 10.17%, Ethylhexyl Methoxycinnamate 3.00%, Zinc Oxide 1.92%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
CYCLOPENTASILOXANE, WATER, ISODODECANE, DIMETHICONE, BUTYLENE GLYCOL, CAPRYLYL METHICONE, ALCOHOL, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, TALC, POLYMETHYLSILSESQUIOXANE, NIACINAMIDE, PEG-10 DIMETHICONE, SYNTHETIC FLUORPHLOGOPITE, IRON OXIDES(CI 77492), DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, ACRYLATES/DIMETHICONE COPOLYMER, PHENOXYETHANOL, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, METHICONE, FRAGRANCE, IRON OXIDES(CI 77491), AMINOPROPYL DIMETHICONE, ETHYLHEXYLGLYCERIN, TOCOPHERYL ACETATE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, ALUMINA, ANGELICA KEISKEI EXTRACT, ANTHEMIS NOBILIS FLOWER EXTRACT, FOENICULUM VULGARE (FENNEL) LEAF EXTRACT, LAURUS NOBILIS LEAF EXTRACT, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER/LEAF/STEM EXTRACT, MENTHA PIPERITA (PEPPERMINT) EXTRACT,
PERILLA OCYMOIDES LEAF EXTRACT, ROSMARINUS OFFICINALIS (ROSEMARY) EXTRACT, IRON OXIDES(CI 77499), ADENOSINE, TRIETHOXYCAPRYLYLSILANE, SILICA, ACRYLATES/TRIDECYL ACRYLATE/TRIETHOXYSILYLPROPYL METHACRYLATE/DIMETHICONE METHACRYLATE COPOLYMER, CELLULOSE, DIMETHICONE/METHICONE COPOLYMER, DIMETHICONOL, GOSSYPIUM HERBACEUM (COTTON) FRUIT WATER

PURPOSE

OTC - PURPOSE SECTION

Purpose: Brightening, Wrinkle-Improvement, UV Protection

Cautions

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

How to Use

INDICATIONS & USAGE SECTION

How to Use:
After applying sun cream or makeup primer, gently shake the bottle and dispense 1-2 drops onto the back of your hands using the fountain pen filler.
Smooth on with foundation brush or your fingertips starting in the center of face, blending outwards.
Make sure the cap is tightly closed and shake 2-3 times before use.

How to Use

DOSAGE & ADMINISTRATION SECTION

How to Use:
After applying sun cream or makeup primer, gently shake the bottle and dispense 1-2 drops onto the back of your hands using the fountain pen filler.
Smooth on with foundation brush or your fingertips starting in the center of face, blending outwards.
Make sure the cap is tightly closed and shake 2-3 times before use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-261-012020-01-31C16284748780-19d75b9d0-a8b2-f424-e053-dadaa90a57ce7445f1cc-572e-4a94-8c24-41c14e3bdfea

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51346-261-01SUPER ORIGIN COTTON FINISH FOUNDATION21 LIGHT BEIGE30 mL in 1 CARTONCREAM301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51346-261SUPER ORIGIN COTTON FINISH FOUNDATION 21 LIGHT BEIGE (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE) CREAM [NATURE REPUBLIC CO., LTD.]1Legacy NDC, 1 package rows20140502_7445f1cc-572e-4a94-8c24-41c14e3bdfea.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
Zinc OxideACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-26151346-261-01

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
Titanium Dioxide15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
Zinc OxideSOI2LOH54ZACTIM
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT

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
ec206b3d-4f77-4f97-bdd4-d6dbaf93f5af7445f1cc-572e-4a94-8c24-41c14e3bdfea2014-05-02WarningsExact identifier
spl id: ec206b3d-4f77-4f97-bdd4-d6dbaf93f5af
spl set id: 7445f1cc-572e-4a94-8c24-41c14e3bdfea

Reported adverse events (FAERS/openFDA)#

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