FDA.reportPublic FDA data

SUPER ORIGIN COLLAGEN WATERPROOF BB

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-08-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:46:11

Label at a glance#

ProductSUPER ORIGIN COLLAGEN WATERPROOF BB SPF46 PA PLUS PLUS PLUS
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE, OCTISALATE
Label structure8 sections

Indications and uses

How to Use: Apply an appropriate amount evenly to the entire face.

Dosage and administration

How to Use: Apply an appropriate amount evenly to the entire face.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethylhexyl Methoxycinnamate 7%, Titanium Dioxide 6.9%, Zinc Oxide 4.9%, Ethylhexyl Salicylate 3%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Triethoxycaprylylsilane, Cyclopentasiloxane, Dimethicone, Cyclohexasiloxane, Butylene Glycol Dicaprylate/Dicaprate, Aluminum Hydroxide, Stearic Acid, PEG-10 Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Butylene Glycol, Phenyl Trimethicone, Niacinamide, Propylene Glycol, Acacia Seyal Gum Extract, Potassium Sorbate, Phenoxyethanol, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, Magnesium Sulfate, Disteardimonium Hectorite, Iron Oxides, Ozokerite, Sorbitan Isostearate, Beeswax, Fragrance, Disodium EDTA,
Tocopheryl Acetate, Adenosine, Aloe Barbadensis Leaf Extract, Camellia Sinensis Leaf Extract, Ethylhexyl Palmitate, Silica Dimethyl Silylate, Caprylyl Glycol, Sodium Hyaluronate, Hexylene Glycol

PURPOSE

OTC - PURPOSE SECTION

Purpose:
Resistant against water, sweat, and UV rays, keeping makeup fresh for long hours.
This product increases elasticity formulated with Acacia flower-derived collagen.
It gives a matt-finished look with healthy skin tone.

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rash 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: Apply an appropriate amount evenly to the entire face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: Apply an appropriate amount evenly to the entire face.

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
51346-052-012021-06-29C16284748780-19d75b9d1-0846-f424-e053-dadaa90a57ceb4080c53-e0d0-41ac-b78e-f241173f5897
51346-052-012020-01-31C16284748780-19d75b9d1-0846-f424-e053-dadaa90a57ceb4080c53-e0d0-41ac-b78e-f241173f5897

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 OXIDEACTIVE MOIETYSOI2LOH54Z1
CYCLOMETHICONE 5INACTIVE INGREDIENT0THT5PCI0R1
CYCLOMETHICONE 6INACTIVE INGREDIENTXHK3U310BA1
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O1
TRIETHOXYCAPRYLYLSILANEINACTIVE INGREDIENTLDC331P08E1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-05251346-052-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIM
TITANIUM DIOXIDE15FIX9V2JPACTIM
ZINC OXIDESOI2LOH54ZACTIM
OCTISALATE4X49Y0596WACTIM
WATER059QF0KO0RIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE92RU3N3Y1OIACT
CYCLOMETHICONE 6XHK3U310BAIACT

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
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RAEROSOL, FOAM / TOPICAL144 mgExact identifier — unii candidate
3 equally ranked IID candidates
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RCREAM, AUGMENTED / TOPICAL260 mgExact identifier — unii candidate
3 equally ranked IID candidates
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RAEROSOL / TOPICAL2.5 %w/wExact 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
34f33636-71ae-4c61-84a3-6001de34a322b4080c53-e0d0-41ac-b78e-f241173f58972021-06-28WarningsExact identifier
spl set id: b4080c53-e0d0-41ac-b78e-f241173f5897

Reported adverse events (FAERS/openFDA)#

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