SUPER ORIGIN CC

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2013-05-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:40:44

Label at a glance#

ProductSUPER ORIGIN CC SPF25 PA PLUS PLUS BRIGHTENING
Active ingredientOCTINOXATE, OCTISALATE, Titanium Dioxide, AVOBENZONE, Homosalate, Octocrylene
Label structure8 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethylhexyl Methoxycinnamate 7.3%, Ethylhexyl Salicylate 4.5%, Titanium Dioxide 3.87%, Butyl Methoxydibenzoylmethane 2.2%, Homosalate 2%, Octocrylene 1%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Cyclopentasiloxane, Dipropylene Glycol, Butylene Glycol, Ethylhexyl Palmitate, Niacinamide, Isoamyl p-Methoxycinnamate, Cyclohexasiloxane, Polysorbate 60, Neopentyl Glycol Diheptanoate, Pentylene Glycol, Triceteareth-4 Phosphate, Glyceryl Stearate,
PEG-100 Stearate, Glycol Stearate, Methyl Methacrylate Crosspolymer, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Silica, Polymethylsilsesquioxane, PEG-2 Stearate, Aluminum Hydroxide, Stearic Acid, Phenoxyethanol, Dimethiconol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Fragrance(Parfum), Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Ammonium Acryloyldimethyltaurate/VP Copolymer, Isohexadecane, Glycerin, Xanthan Gum, Caffeine, Adenosine, Polysorbate 80, Disodium EDTA, Allantoin, Triethoxycaprylylsilane, Ceramide 3, Ascorbyl Glucoside, Hydrolyzed Collagen, Iron Oxides (CI 77491), Rosa Canina Fruit Extract, Hibiscus Sabdariffa Flower Extract, Lavandula Angustifolia (Lavender) Flower Extract, Cymbopogon Schoenanthus Leaf Extract, Melissa Officinalis Extract,
Rosmarinus Officinalis (Rosemary) Leaf Extract, Tilia Europaea Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Thymus Vulgaris (Thyme) Leaf Extract, Lippia Citriodora Leaf Extract, Rosa Damascena Flower Extract

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes and mouth.
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

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

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

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use:
At the last step of skincare, apply an appropriate amount to the entire face.
As this product has a UV Protection function, 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-215-012021-07-02C16284748780-19d75b9d0-ec23-f424-e053-dadaa90a57ce70506102-a3c7-48f5-abca-c3752b1af96d
51346-215-012020-01-31C16284748780-19d75b9d0-ec23-f424-e053-dadaa90a57ce70506102-a3c7-48f5-abca-c3752b1af96d

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
HomosalateACTIVE INGREDIENTV06SV4M95S1
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
HOMOSALATEACTIVE MOIETYV06SV4M95S1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-21551346-215-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
dfa18363-d661-4366-8624-c4b377a69fe770506102-a3c7-48f5-abca-c3752b1af96d2021-07-02WarningsExact identifier
spl set id: 70506102-a3c7-48f5-abca-c3752b1af96d

Reported adverse events (FAERS/openFDA)#

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