WHITE VITA FLORAL TONER- niacinamide liquid

WHITE VITA FLORAL TONER by

Drug Labeling and Warnings

WHITE VITA FLORAL TONER by is a Otc medication manufactured, distributed, or labeled by NATURE REPUBLIC CO., LTD., Kolmar Korea Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS: NIACINAMIDE 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: WATER,PROPANEDIOL,ALCOHOL,PEG/PPG-17/6 COPOLYMER,PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT,ALOE BARBADENSIS LEAF JUICE,DIOSCOREA JAPONICA ROOT EXTRACT,1,2-HEXANEDIOL,SOLUBLE COLLAGEN,BETAINE,PHENOXYETHANOL,HYDROGENATED LECITHIN,ARCTIUM LAPPA ROOT EXTRACT,PHELLINUS LINTEUS EXTRACT

PURPOSE

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

CAUTIONS

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

KEEP OUT OF REACH OF CHILDREN

HOW TO USE

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. It is recommended to apply after first essence.

HOW TO USE

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. It is recommended to apply after first essence.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WHITE VITA FLORAL TONER 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-371
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	3.0 g  in 150 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPANEDIOL (UNII: 5965N8W85T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-371-01	150 mL in 1 CARTON; Type 0: Not a Combination Product	11/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/01/2015

Labeler - NATURE REPUBLIC CO., LTD. (631172020)

Registrant - NATURE REPUBLIC CO., LTD. (631172020)

Establishment
Name	Address	ID/FEI	Business Operations
NATURE REPUBLIC CO., LTD.		631172020	relabel(51346-371)

Establishment
Name	Address	ID/FEI	Business Operations
Kolmar Korea Co., Ltd.		689512611	manufacture(51346-371)