FDA.reportPublic FDA data

PURE BB 21 LIGHT BEIGE

Manufacturer
NATURE REPUBLIC CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong Factory
Effective date
2019-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:47:41

Label at a glance#

ProductPURE BB 21 LIGHT BEIGE
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE
Label structure7 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: TITANIUM DIOXIDE 9.40%, ETHYLHEXYL METHOXYCINNAMATE 6.00%, ETHYLHEXYL SALICYLATE 2.00%, ZINC OXIDE 1.92%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER,CYCLOPENTASILOXANE,TITANIUM DIOXIDE,ETHYLHEXYL METHOXYCINNAMATE,GLYCERIN,CETYL ETHYLHEXANOATE,ISOSTEARYL ISOSTEARATE,METHYL TRIMETHICONE,PROPYLENE GLYCOL,CETYL PEG/PPG-10/1 DIMETHICONE,TALC,CAPRYLYL METHICONE,ETHYLHEXYL SALICYLATE,NIACINAMIDE,ZINC OXIDE,DIMETHICONE,IRON OXIDES(CI 77492),DISTEARDIMONIUM HECTORITE,PEG-10 DIMETHICONE,SILICA,MAGNESIUM SULFATE,PORTULACA OLERACEA EXTRACT,ACRYLATES/ETHYLHEXYL ACRYLATE/DIMETHICONE METHACRYLATE COPOLYMER,MICA,PHENOXYETHANOL,POLYGLYCERYL-4 ISOSTEARATE,METHICONE,BEESWAX,IRON OXIDES(CI 77491),ALUMINUM HYDROXIDE,AMINOPROPYL DIMETHICONE,ALUMINUM STEARATE,FRAGRANCE,POLYMETHYLSILSESQUIOXANE,ETHYLHEXYLGLYCERIN,TOCOPHERYL ACETATE,ALUMINA,POLYURETHANE-11,IRON OXIDES(CI 77499),ADENOSINE,HELICHRYSUM ITALICUM FLOWER WATER,HIBISCUS SABDARIFFA FLOWER EXTRACT,BUTYLENE GLYCOL,BUDDLEJA DAVIDII EXTRACT,THYMUS VULGARIS (THYME) EXTRACT,DIANTHUS CHINENSIS EXTRACT,NELUMBO NUCIFERA FLOWER EXTRACT,OCIMUM BASILICUM (BASIL) FLOWER/LEAF/STEM EXTRACT,ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT,EUCALYPTUS GLOBULUS LEAF EXTRACT

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen [UV Protection, Brightening, Wrinkle-Improvement]

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.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

HOW TO USE

DESCRIPTION SECTION

HOW TO USE: At the last step of skin care, apply an appropriate amount to the entire face in a gentle tapping motion to achieve natural makeup

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of cartonImage of cartonImage of carton

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
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-29151346-291-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
ZINC OXIDESOI2LOH54ZACTIM
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
8d2d4f18-1cca-403f-83ed-920f2fbec5cac758b567-7671-4164-9298-e52f5bdfdbbd2019-12-31WarningsExact identifier
spl id: 8d2d4f18-1cca-403f-83ed-920f2fbec5ca
spl set id: c758b567-7671-4164-9298-e52f5bdfdbbd

Reported adverse events (FAERS/openFDA)#

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