SFERANGS VITA C CAPSULEBOOSTER- niacinamide liquid

SFERANGS VITA C CAPSULEBOOSTER by

Drug Labeling and Warnings

SFERANGS VITA C CAPSULEBOOSTER 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

INACTIVE INGREDIENT

Water
Anthemis Nobilis Flower Extract
Ascorbic Acid
Sodium Citrate
Dipropylene Glycol
Butylene glycol
Propylene Glycol
Alcohol
Glycereth-26
PEG-400
Glycolic acid
PPG-26-Buteth-26
PEG-40 Hydrogenated Castor Oil
Xanthan GUM
Dipotassium Glycyrrhizate
Algin
Disodium EDTA
Acanthopanax Senticosus (Eleuthero) Root Extract
Punica Granatum Fruit Extract
Panax Ginseng Root Extract
Carthamus Tinctorius (Safflower) Flower Extract
Aloe vera Callus Culture extracts
Camellia sinensis Callus Culture extracts
Phenoxyethanol
Ethylhexylglycerin
Parfum

PURPOSE

anti-wrinkle

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

apply proper amount to the skin

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SFERANGS VITA C CAPSULEBOOSTER 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73590-0041
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73590-0041-1	10 mL in 1 AMPULE; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/08/2020

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(73590-0041)