Magnolia Serum

Manufacturer: Grace & Truth Co.,Ltd.
Effective date: 2020-12-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:35:53

Label at a glance#

ProductMagnolia Serum

Active ingredientMAGNOLIA KOBUS FLOWERING TOP

Label structure8 sections

Indications and uses

This whitening serum brightens and monetarizes naturally for radiant looking.

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Magnolia Kobus Flower Extract 14.56%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Skin Brightening

WARNINGS

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Uses

INDICATIONS & USAGE SECTION

This whitening serum brightens and monetarizes naturally for radiant looking.

Directions

DOSAGE & ADMINISTRATION SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81355-100-02	2023-07-28	C162847	48780-1	0191ceaa-6b69-198a-e063-dbdaa90aec3e	dbfb2a3d-3efb-45bf-87ba-3bce145919d9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81355-100-01	Magnolia Serum	30 mL in 1 BOTTLE	LIQUID	30		1
81355-100-02	Magnolia Serum	1 in 1 CARTON	LIQUID	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81355-100	MAGNOLIA SERUM (MAGNOLIA KOBUS FLOWER) LIQUID [GRACE & TRUTH CO.,LTD.]	1	Legacy NDC, 2 package rows	20201225_dbfb2a3d-3efb-45bf-87ba-3bce145919d9.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Magnolia Serum
Magnolia Kobus Flower
MAGNOLIA KOBUS FLOWERING TOP
Water
Arbutin

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81355-100	81355-100-01, 81355-100-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MAGNOLIA KOBUS FLOWERING TOP	X2725LP5TL	ACTIB
Water	059QF0KO0R	IACT
Arbutin	C5INA23HXF	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f7862980-c2e3-461e-a616-d7443337f8ac			dbfb2a3d-3efb-45bf-87ba-3bce145919d9	2020-12-24	Warnings	Exact identifier spl id: f7862980-c2e3-461e-a616-d7443337f8ac spl set id: dbfb2a3d-3efb-45bf-87ba-3bce145919d9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.