MAGNOLIA SERUM- magnolia kobus flower liquid

Magnolia Serum by

Drug Labeling and Warnings

Magnolia Serum by is a Otc medication manufactured, distributed, or labeled by Grace & Truth Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Magnolia Kobus Flower Extract 14.56%

INACTIVE INGREDIENTS

Purified water, Orostachys Japonica Extract, Ginkgo Biloba Leaf Extract, Cnidium Officinale Rhizome Extract, Poria Cocos Extract, Gardenia Florida Flower Extract, Paeonia Suffruticosa Root Extract, Dandelion Leaf Extract, Morus Alba Leaf Extract, Houttuynia Cordata Extract, Arbutin, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Ferment Extract, Coffee Robusta Seed Extract, Lavander Oil

PURPOSE

Skin Brightening

WARNINGS

For external use only. Avoid contact with eyes. 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

Uses

This whitening serum brightens and monetarizes naturally for radiant looking.

Directions

Pat on your face right after cleansing in the morning and in the evening. 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MAGNOLIA SERUM 
magnolia kobus flower liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81355-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MAGNOLIA KOBUS FLOWERING TOP (UNII: X2725LP5TL) (MAGNOLIA KOBUS FLOWERING TOP - UNII:X2725LP5TL)	MAGNOLIA KOBUS FLOWERING TOP	4.36 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Arbutin (UNII: C5INA23HXF)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81355-100-02	1 in 1 CARTON	12/01/2020
1	NDC: 81355-100-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/01/2020

Labeler - Grace & Truth Co.,Ltd. (695160801)

Registrant - Grace & Truth Co.,Ltd. (695160801)

Establishment
Name	Address	ID/FEI	Business Operations
Grace & Truth Co.,Ltd.		695160801	manufacture(81355-100)