FDA.reportPublic FDA data

NATURE ORIGIN CUSHION CC NATURAL

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc.
Effective date
2019-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:47:30

Label at a glance#

ProductNATURE ORIGIN CUSHION CC NATURAL NO.21
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Titanium Dioxide (CI 77891) (10.9%) - SUNSCREEN Ethylhexyl Methoxycinnamate (6.7%) - SUNSCREEN Ethylhexyl Salicylate (4%) - SUNSCREEN

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Water, Cyclopentasiloxane, Butylene Glycol, Caprylyl Methicone, PEG-10 Dimethicone, Glycerin, Niacinamide, Diphenylsiloxy Phenyl Trimethicone, Butylene Glycol Dicaprylate/Dicaprate, Pentylene Glycol, PEG-8 Dimethicone, Dimethicone, Mica (CI 77019), PEG-8, HDI/Trimethylol Hexyllactone Crosspolymer, Iron Oxides (CI 77492), Phenoxyethanol, Magnesium Sulfate, Diphenyl Dimethicone, Acrylates/Stearyl Acrylate/Dimethicone Methacrylate Copolymer, Trimethylsiloxysilicate,Dimethicone Crosspolymer, Cyclohexasiloxane, Stearic Acid, Disteardimonium Hectorite, Alumina, Dimethicone/Vinyl Dimethicone Crosspolymer, Iron Oxides (CI 77491), Fragrance(Parfum), Triethoxycaprylylsilane, Aluminum Hydroxide, Ethylhexylglycerin, Iron Oxides (CI 77499), Adenosine, Disodium EDTA, Silica, Ceramide 3, Ascorbic Acid, Soluble Collagen

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

WARNINGS

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. After use, close the cap tightly to prevent the product from degradation and evaporation.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

HOW TO USE : Take an adequate amount by gently pressing the sponge with the puff, and apply thinly to the face. Gently pat to adhere to the skin. Apply as needed after wearing makeup.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

HOW TO USE : Take an adequate amount by gently pressing the sponge with the puff, and apply thinly to the face. Gently pat to adhere to the skin. Apply as needed after wearing makeup.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

Image of cartonImage of carton

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-271-012021-07-13C16284748780-1ba0f9c33-2b8d-a910-e053-dadaa90a0b8563812aa0-bcb8-4908-8b31-a2a0b6dd9bdc
51346-271-012021-01-29C16284748780-1ba0f9c33-2b8d-a910-e053-dadaa90a0b8563812aa0-bcb8-4908-8b31-a2a0b6dd9bdc

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-27151346-271-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
Water059QF0KO0RIACT

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
2b21ed20-090b-4427-8121-50c9b2f2ac3763812aa0-bcb8-4908-8b31-a2a0b6dd9bdc2021-07-13WarningsExact identifier
spl set id: 63812aa0-bcb8-4908-8b31-a2a0b6dd9bdc

Reported adverse events (FAERS/openFDA)#

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