WHITE VITA FLORAL ESSENCE

Manufacturer
NATURE REPUBLIC CO., LTD. | Kolmar Korea Co., Ltd.
Effective date
2017-02-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:19:05

Label at a glance#

ProductWHITE VITA FLORAL ESSENCE BRIGHTENING
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: NIACINAMIDE 5.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER, METHYLPROPANEDIOL, BETAINE, CAPRYLIC/CAPRIC TRIGLYCERIDE, DIOSCOREA JAPONICA ROOT EXTRACT, 1,2-HEXANEDIOL, PENTYLENE GLYCOL, BIFIDA FERMENT LYSATE, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, ARCTIUM LAPPA ROOT EXTRACT, PANTHENOL, PHELLINUS LINTEUS EXTRACT, TRANEXAMIC ACID, HYDROGENATED LECITHIN, GELATIN, TROMETHAMINE, ETHYLHEXYLGLYCERIN, POLYQUATERNIUM-51, OLEA EUROPAEA (OLIVE) LEAF EXTRACT, PANCRATIUM MARITIMUM EXTRACT, NYMPHAEA ALBA FLOWER EXTRACT, GLYCOSYL TREHALOSE, GLYCERIN, CELLULOSE GUM, FRAGRANCE, HYDROGENATED STARCH HYDROLYSATE, BIOSACCHARIDE GUM-1, RAFFINOSE, DISODIUM EDTA, LECITHIN, SODIUM HYALURONATE, PEG-60 HYDROGENATED CASTOR OIL, CARBOMER, PEG-40 HYDROGENATED CASTOR OIL, BUTYLENE GLYCOL, CALCIUM ALGINATE, AGAR, GELLAN GUM, PROPANEDIOL, ACETIC ACID, DIPROPYLENE GLYCOL, LACTIC ACID, ASCORBYL GLUCOSIDE, ZINC PCA, SODIUM PALMITOYL PROLINE, INOSITOL, ARGANIA SPINOSA KERNEL OIL, BISABOLOL, TETRAHEXYLDECYL ASCORBATE, TOCOPHERYL ACETATE, ASCORBIC ACID, BIOFLAVONOIDS, HESPERIDIN, RETINYL PALMITATE, TOCOPHEROL, PHENOXYETHANOL, POTASSIUM SORBATE

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: [BRIGHTENING & SKIN MOISTURIZING] This capsule essence delivers moisture to skin while clarifying and purifying the skin.

CAUTIONS

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

HOW TO USE

INDICATIONS & USAGE SECTION

HOW TO USE: Use at the next step of emulsion. Apply an appropriate amount on the entire face in a tapping motion to promote absorption into skin.

HOW TO USE

DOSAGE & ADMINISTRATION SECTION

HOW TO USE: Use at the next step of emulsion. Apply an appropriate amount on the entire face in a tapping motion to promote absorption into skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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
51346-37351346-373-01

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
WATER059QF0KO0RIACT
METHYLPROPANEDIOLN8F53B3R4RIACT

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
179315cf-4848-4bcc-ae0c-29d7df90ff6684d40cbe-1308-4ac4-9ca3-ce38f1aadd162021-07-07WarningsExact identifier
spl set id: 84d40cbe-1308-4ac4-9ca3-ce38f1aadd16

Reported adverse events (FAERS/openFDA)#

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