POWER GEMSTONE

Manufacturer: Myeong SA
Effective date: 2020-01-16
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:02:55

Label at a glance#

ProductPOWER GEMSTONE

Active ingredientPANAX GINSENG WHOLE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ginseng

INACTIVE INGREDIENT SECTION

Magnolia officinalis, cinnamon, Gleditsia japonica, barberry root, Asteris Radix, ballon flower, Zingiber officinale, japanese aconite root

OTC - PURPOSE SECTION

prevention and treatment of Atopy, allergy, rhinitis

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children

INDICATIONS & USAGE SECTION

6 times a day (Every 4 hours)

Dose: 4g

WARNINGS SECTION

Take the appropriate amount.

If any of symptoms occur, consult with your doctor or pharmacist.

DOSAGE & ADMINISTRATION SECTION

6 times a day

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71960-0003-1	2021-07-23	C162847	48780-1	c7ccaba7-0ef4-fd44-e053-dadaa90aa01b	734cd871-42e3-38e6-e053-2a91aa0ae962

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71960-0003-1	POWER GEMSTONE	300 g in 1 BOTTLE, PLASTIC	PILL	300		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71960-0003	POWER GEMSTONE (GINSENG) PILL [MYEONG SA]	2	Legacy NDC, 1 package rows	20200117_734cd871-42e3-38e6-e053-2a91aa0ae962.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

POWER GEMSTONE
ginseng
MAGNOLIA OFFICINALIS WHOLE
PANAX GINSENG WHOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71960-0003	71960-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MAGNOLIA OFFICINALIS WHOLE	9OB542Y2EX	IACT
PANAX GINSENG WHOLE	9L5JEP7MES	ACTIM

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
9c4f51da-ef56-2806-e053-2a95a90a61b4			734cd871-42e3-38e6-e053-2a91aa0ae962	2020-01-16	Warnings	Exact identifier spl id: 9c4f51da-ef56-2806-e053-2a95a90a61b4 spl set id: 734cd871-42e3-38e6-e053-2a91aa0ae962

Reported adverse events (FAERS/openFDA)#

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