NATURE ORIGIN CC BRIGHTENING

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc
Effective date
2017-02-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:19:21

Label at a glance#

ProductNATURE ORIGIN CC BRIGHTENING
Active ingredientOctinoxate, Titanium Dioxide, Octisalate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Ethylhexyl Methoxycinnamate 6.70%, Titanium Dioxide 3.57%, Ethylhexyl Salicylate 2.50%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water,Butylene Glycol,Glycerin,Cyclopentasiloxane,Cyclohexasiloxane,Niacinamide,Dicaprylyl Carbonate,Cetyl Ethylhexanoate,Octyldodecanol,Pentylene Glycol,Diethylamino Hydroxybenzoyl Hexyl Benzoate,Diphenylsiloxy Phenyl Trimethicone,Triceteareth-4 Phosphate,Glycol Stearate,Phenoxyethanol,Glyceryl Stearate,Potassium Cetyl Phosphate,PEG-2 Stearate,PEG-100 Stearate,Mica (CI 77019),PEG-10 Dimethicone,Carbomer,Triethanolamine,Aluminum Hydroxide,Stearic Acid,Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer,Fragrance(Parfum),Isohexadecane,Ethylhexylglycerin,Xanthan Gum,Triethoxycaprylylsilane,Adenosine,Polysorbate 80,Iron Oxides (CI 77492),Disodium EDTA,Iron Oxides (CI 77491),Sorbitan Oleate,Argania Spinosa Kernel Oil,Ascorbyl Glucoside,Hydrolyzed Collagen,Moringa Pterygosperma Seed Extract,Maltodextrin,Cananga Odorata Flower Extract,Lippia Citriodora Leaf Extract,Lavandula Angustifolia (Lavender) Flower Water,Rosmarinus Officinalis (Rosemary) Leaf Water,Mentha Rotundifolia Leaf Extract,Chamomilla Recutita (Matricaria) Flower Water,Mentha Piperita (Peppermint) Leaf Water,Hibiscus Sabdariffa Flower Extract,Jasminum Officinale (Jasmine) Flower Water,Ceramide 3,Salvia Officinalis (Sage) Leaf Extract,Sodium Benzoate,Citric Acid

PURPOSE

OTC - PURPOSE SECTION

Purpose: [SUNSCREEN] Illumination CC for a gorgeously shine skin.

Cautions

WARNINGS SECTION

Cautions: 1. For external use only 2. Avoid contact with eyes and mouth 3. Discontinue use if signs of irritation or rashes appear 4. Keep out of reach of children 5. Replace the cap after use

How to use

DESCRIPTION SECTION

How to use: At the last step of skincare, apply an appropriate amount to the entire face. As this has a UV protection, you do not need to apply sun protection cream separately. For an increased coverage, you may apply BB cream or foundation together.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-357-012021-06-23C16284748780-1ba0f9c33-40b9-a910-e053-dadaa90a0b8579cc3417-0dac-491f-8b6c-452a12b63496
51346-357-012021-01-29C16284748780-1ba0f9c33-40b9-a910-e053-dadaa90a0b8579cc3417-0dac-491f-8b6c-452a12b63496

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OctinoxateACTIVE INGREDIENT4Y5P7MUD511
OctisalateACTIVE INGREDIENT4X49Y0596W1
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1
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
51346-35751346-357-01

Ingredients#

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

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

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
31ef3e6a-e92f-46ff-bbed-bc644f36f19079cc3417-0dac-491f-8b6c-452a12b634962021-06-23WarningsExact identifier
spl set id: 79cc3417-0dac-491f-8b6c-452a12b63496

Reported adverse events (FAERS/openFDA)#

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