WHITE VITA FIRST ESSENCE

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2016-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:27:45

Label at a glance#

ProductWHITE VITA FIRST ESSENCE
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: NIACINAMIDE 2.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: SACCHAROMYCES FERMENT, METHYLPROPANEDIOL, PROPANEDIOL, BETAINE, 1,2-HEXANEDIOL, ARCTIUM LAPPA ROOT EXTRACT, PHELLINUS LINTEUS EXTRACT, DIOSCOREA JAPONICA ROOT EXTRACT, HYDROGENATED LECITHIN, WATER, GLYCERIN, PHENOXYETHANOL, SODIUM CITRATE, PANCRATIUM MARITIMUM EXTRACT, NYMPHAEA ALBA FLOWER EXTRACT, OLEA EUROPAEA (OLIVE) LEAF EXTRACT, BIFIDA FERMENT LYSATE, ETHYLHEXYLGLYCERIN, FRAGRANCE, CITRIC ACID, POLYQUATERNIUM-51, GLYCOSYL TREHALOSE, SODIUM HYALURONATE, PEG-40 HYDROGENATED CASTOR OIL, HYDROGENATED STARCH HYDROLYSATE, BIOSACCHARIDE GUM-1, RAFFINOSE, BUTYLENE GLYCOL, LECITHIN, DIPROPYLENE GLYCOL, SODIUM PALMITOYL PROLINE, BISABOLOL, ARGANIA SPINOSA KERNEL OIL, ACETIC ACID, LACTIC ACID, ASCORBYL GLUCOSIDE, DICAPRYLYL CARBONATE, ZINC PCA, SUCROSE DISTEARATE, CERAMIDE NP, ASCORBIC ACID, BIOFLAVONOIDS, HESPERIDIN, RETINYL PALMITATE, TOCOPHEROL, POTASSIUM SORBATE

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: [Skin protectant] The extract type essence that provides rich nourishment to the skin

CAUTIONS

WARNINGS SECTION

CAUTIONS: 1. For external use only 2. Avoid contact with eyes. 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

INDICATIONS & USAGE SECTION

HOW TO USE: After washing the face, dispense an appropriate amount onto a cotton pad and gently cleanse the skin along skin’s texture starting from the inside and working outward; pat to promote absorption into skin.

HOW TO USE

DOSAGE & ADMINISTRATION SECTION

HOW TO USE: After washing the face, dispense an appropriate amount onto a cotton pad and gently cleanse the skin along skin’s texture starting from the inside and working outward; pat to promote absorption into skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-380-012021-07-07C16284748780-19d75b9cf-f332-f424-e053-dadaa90a57ceec9edb19-be39-4fe0-8638-17bf03d97010
51346-380-012020-01-31C16284748780-19d75b9cf-f332-f424-e053-dadaa90a57ceec9edb19-be39-4fe0-8638-17bf03d97010

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-38051346-380-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4ACTIB
METHYLPROPANEDIOLN8F53B3R4RIACT
PROPANEDIOL5965N8W85TIACT

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
a44f8377-65be-424c-a632-160be738b2bbec9edb19-be39-4fe0-8638-17bf03d970102021-07-07WarningsExact identifier
spl set id: ec9edb19-be39-4fe0-8638-17bf03d97010

Reported adverse events (FAERS/openFDA)#

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