PURE SHINE VANILLA MAKEUP BASE 02 VANILLA PINK

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmecca Korea Co., Ltd.
Effective date
2017-02-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:19:23

Label at a glance#

ProductPURE SHINE VANILLA MAKEUP BASE 02 VANILLA PINK
Active ingredientTitanium Dioxide, Octinoxate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: Titanium Dioxide (CI 77891) 5.03%, Ethylhexyl Methoxycinnamate 2.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Water,Cyclopentasiloxane,Phenyl Trimethicone,Butylene Glycol,Cyclohexasiloxane,4-Methylbenzylidene Camphor,Glycerin,Sodium Chloride,Cetyl PEG/PPG-10/1 Dimethicone,Polyglyceryl-4 Isostearate,Sorbitan Isostearate,Hexyl Laurate,Dimethicone,Disteardimonium Hectorite,Sorbitan Olivate,Dimethicone/Vinyl Dimethicone Crosspolymer,Beeswax,Calcium Stearate,Butylene Glycol Dicaprylate/Dicaprate,Ozokerite,Chromium Oxide Greens,Tocopheryl Acetate,Propylene Carbonate,Propylparaben,Methylparaben,Fragrance,Quaternium-18 Bentonite,Disodium EDTA, Triethanolamine, Triethoxycaprylylsilane , Alcohol, Silica, Vanilla Planifolia Fruit extract, Phenoxyethanol, Sodium Hyaluronate, Ethylhexylglycerin

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Keep out of reach of children

DESCRIPTION

DESCRIPTION SECTION

Indications & Usage: Makeup base that evens out the skin tone.

Dosage & Administration: Apply an adequate amount to skin using either hand or puff.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of tubeImage of tube

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-461-012020-02-19C16284748780-19d75b9d0-ada7-f424-e053-dadaa90a57cef8a2ebf6-0629-42b2-a460-b99db51b42c6
51346-461-012020-01-31C16284748780-19d75b9d0-ada7-f424-e053-dadaa90a57cef8a2ebf6-0629-42b2-a460-b99db51b42c6

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-46151346-461-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
e5b2adbe-dd88-4413-af40-b29074a7bd98f8a2ebf6-0629-42b2-a460-b99db51b42c62017-02-17WarningsExact identifier
spl id: e5b2adbe-dd88-4413-af40-b29074a7bd98
spl set id: f8a2ebf6-0629-42b2-a460-b99db51b42c6

Reported adverse events (FAERS/openFDA)#

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