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 01:40:43

Label at a glance#

ProductSUPER ORIGIN CC SPF30 PA PLUS PLUS COLOR CHANGE
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE
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 seperately. 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 seperately. 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: TITANIUM DIOXIDE 6.35%, ETHYLHEXYL METHOXYCINNAMATE 6%, ETHYLHEXYL SALICYLATE 2%, ZINC OXIDE 1.92%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
WATER, CYCLOPENTASILOXANE, DIPROPYLENE GLYCOL, GLYCERIN, ISOPROPYL ISOSTEARATE, PEG-10 DIMETHICONE, NIACINAMIDE, TALC, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, IRON OXIDES(CI77492), DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, DIMETHICONE, C12-14 PARETH-3, PORTULACA OLERACEA EXTRACT, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, MICA, IRON OXIDES(CI77491), PHENOXYETHANOL, GLYCOSYL TREHALOSE, PALMITIC ACID, TRIHYDROXYSTEARIN, ALUMINUM HYDROXIDE, SILICA DIMETHYL SILYLATE, IRON OXIDES(CI77499), ALUMINUM STEARATE, METHICONE, POLYESTER-1, HYDROGENATED STARCH HYDROLYSATE, TOCOPHERYL ACETATE, ETHYLHEXYLGLYCERIN, FRAGRANCE, HAMAMELIS VIRGINIANA FLOWER WATER, SOLUBLE COLLAGEN, TILIA VULGARIS FLOWER EXTRACT, ROSMARINUS OFFICINALIS (ROSEMARY) EXTRACT, LAURUS NOBILIS LEAF EXTRACT, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER/LEAF/STEM EXTRACT, MENTHA PIPERITA (PEPPERMINT) EXTRACT, ADENOSINE, ASCORBYL GLUCOSIDE, BUTYLENE GLYCOL, AMINOPROPYL DIMETHICONE, POLYMETHYLSILSESQUIOXANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, HYDROGENATED LECITHIN,
BETA-GLUCAN, CERAMIDE 3, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, MELISSA OFFICINALIS EXTRACT, VISCUM ALBUM (MISTLETOE) EXTRACT, CHOLESTEROL

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 seperately.
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 seperately.
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
51346-217-012021-06-22C16284748780-19d75b9d0-94a5-f424-e053-dadaa90a57ce16246ed0-6517-4975-80aa-314af8aaf6d4
51346-217-012020-01-31C16284748780-19d75b9d0-94a5-f424-e053-dadaa90a57ce16246ed0-6517-4975-80aa-314af8aaf6d4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
DIPROPYLENE GLYCOLINACTIVE INGREDIENTE107L85C401
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
51346-21751346-217-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

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 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
3 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 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
99e4fb9d-c8b0-4971-a37c-ae629328e9aa16246ed0-6517-4975-80aa-314af8aaf6d42021-06-22WarningsExact identifier
spl set id: 16246ed0-6517-4975-80aa-314af8aaf6d4

Reported adverse events (FAERS/openFDA)#

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