TAEYANGSOO PLAVITALEMULSION- adenosine, niacinamide emulsion

TAEYANGSOO PlavitalEmulsion by

Drug Labeling and Warnings

TAEYANGSOO PlavitalEmulsion by is a Otc medication manufactured, distributed, or labeled by Unimed Pharmaceuticals, Inc., C&T Dream. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

adenosine, niacinamide

INACTIVE INGREDIENT

Camellia Sinensis Leaf Water
1,2-Hexanediol
Propanediol
Water
Hydrolyzed Placental Extract
1,2-Hexanediol
Glycereth-26
Glycerin
Water
1,2-Hexanediol
Glycyrrhiza Uralensis (Licorice) Root Extract
1,2-Hexanediol
Betaine
Beta-Glucan
Water
1,2-Hexanediol
Paeonia Albiflora Root Extract
Bis-PEG-18 Methyl Ether Dimethyl Silane
Water
1,2-Hexanediol
Nelumbium Speciosum Flower Extract
PEG-60 Hydrogenated Castor Oil
Water
1,2-Hexanediol
Honey Extract
Water
1,2-Hexanediol
Portulaca Oleracea Extract
Methylpropanediol
Acrylates/C10-30 Alkyl Acrylate Crosspolymer
Arginine
Ethylhexylglycerin
Sodium Hyaluronate
Disodium EDTA
Water
Scutellaria Baicalensis Root Extract
Glycyrrhiza Glabra (Licorice) Root Extract
Cimicifuga Racemosa Root Extract
Polygonum Multiflorum Root Extract
Sesamum Indicum (Sesame) Seed Extract
Phellinus Linteus Extract
Angelica Gigas Root Extract
Morus Alba Bark Extract
Paeonia Albiflora Root Extract
Sophora Angustifolia Root Extract
1,2-Hexanediol
Phenyl Trimethicone
Fragrance

PURPOSE

anti-wrinkle, whitening

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

external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TAEYANGSOO PLAVITALEMULSION 
adenosine, niacinamide emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73669-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.3 g  in 100 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.04 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: 73669-001-01	78 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/24/2020

Labeler - Unimed Pharmaceuticals, Inc. (689852052)

Registrant - Unimed Pharmaceuticals, Inc. (689852052)

Establishment
Name	Address	ID/FEI	Business Operations
Unimed Pharmaceuticals, Inc.		689852052	label(73669-001)

Establishment
Name	Address	ID/FEI	Business Operations
C&T Dream		694699750	manufacture(73669-001)