VITA C BRIGHT TONER- niacinamide liquid

Vita C Bright Toner by

Drug Labeling and Warnings

Vita C Bright Toner by is a Otc medication manufactured, distributed, or labeled by NOKSIBCHO cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

niacinamide, vitamins, vitamin E

INACTIVE INGREDIENT

Water
Butylene glycol
Glycerin
Dipropylene Glycol
Niacinamide
Alcohol
Saccharide Isomerate
Sodium Hyaluronate
Hydrolyzed Collagen
PPG-26-Buteth-26
PEG-40 Hydrogenated Castor Oil
Methyl Gluceth-20
Glycerin
Glyceryl Acrylate/Acrylic Acid Copolymer
Propylene Glycol
PVM/MA Copolymer
Triethanolamine
Dipotassium Glycyrrhizate
Solanum Lycopersicum (Tomato) Fruit Extract
Paeonia Lactiflora Bark/Sap Extract
Lonicera Japonica (Honeysuckle) Flower Extract
Paullinia Cupana Extract
Euterpe Oleracea Fruit Extract
Panax Ginseng Root Extract
Aloe Barbadensis Leaf Extract
Camellia Sinensis Leaf Extract
Honey
Rosa Multiflora Fruit Extract
Gardenia Florida Fruit Extract
Scutellaria Baicalensis Root Extract
Ligustrum Japonicum Fruit Extract
Carbomer
Tocopheryl Acetate
Disodium EDTA
Carbomer
Panthenol
Betaine
Phaseolus Radiatus Meristem Cell Culture Extract
Camellia Sinensis Callus Culture Extract
Thymus Vulgaris (Thyme) Extract
Buddleja Davidii Extract
Ascorbic Acid
Phenoxyethanol
Ethylhexylglycerin
Parfum

PURPOSE

hyperpigmentation care

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

apply proper amount and gently massage

WARNINGS

For external use only
When using this product

■ if the following symptoms occurs after use, stop use and consult with a skin specialist

red specks, swelling, itching

■ don’t use on the part where there is injury, eczema, or dermatitis

Keep out of reach of children

■ if swallowed, get medical help or contact a person control center immediately

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VITA C BRIGHT TONER 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73590-0018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73590-0018-1	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/14/2020

Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175)

Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175)

Establishment
Name	Address	ID/FEI	Business Operations
NOKSIBCHO cosmetic Co., Ltd.		690182175	manufacture(73590-0018)