Mugwort patch

Manufacturer: Yiwu Quyan E-commerce Trading Co., Ltd.
Effective date: 2024-08-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:17:10

Label at a glance#

ProductMugwort patch

Active ingredientARTEMISIA PRINCEPS LEAF

Label structure14 sections

Dosage and administration

Clean and dry the affected area. Remove the glue and apply it to the sore area. Use no more than eight hours at a time, once a day at most

Storage and handling

Clean and dry the affected area. Remove the glue and apply it to the sore area. Use no more than eight hours at a time, once a day at most

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Mugwort Extract 70%

Purpose

OTC - PURPOSE SECTION

Ease the pain

Use

INDICATIONS & USAGE SECTION

For muscle and joint pain, blood circulation and inflammation

Warnings

WARNINGS SECTION

For external use only. Avoid contact with the eyes, mouth and mucous membranes. Stop use immediately and consult your doctor if you experience redness, itching, or other allergic reactions. Pregnant and lactating women should consult a doctor before using.

Do not use

OTC - DO NOT USE SECTION

Stop use immediately and consult your doctor if you experience redness, itching, or other allergic reactions.

When Using

OTC - WHEN USING SECTION

Avoid contact with the eyes, mouth and mucous membranes. Discontinue use immediately if feeling unwell.

Stop Use

OTC - STOP USE SECTION

Stop use immediately and consult your doctor if you experience redness, itching, or other allergic reactions

Ask Doctor

OTC - ASK DOCTOR SECTION

Pregnant and lactating women should consult a doctor before using.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep this product out of reach of children. If accidentally ingested, please call the emergency center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean and dry the affected area. Remove the glue and apply it to the sore area. Use no more than eight hours at a time, once a day at most

Other information

STORAGE AND HANDLING SECTION

Clean and dry the affected area. Remove the glue and apply it to the sore area. Use no more than eight hours at a time, once a day at most

Inactive ingredients

INACTIVE INGREDIENT SECTION

ginger essential oil,Chuanxiong,Chuangucao,frankincense,Shannai kudzu root,Angelica dahurica

Questions

OTC - QUESTIONS SECTION

86-15797813020

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
84640-001-01	2025-07-29	C162847	48780-1	3b156c62-293f-fb37-e063-e6dba90a4e07	84640-001

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84640-001-01	Mugwort patch	40 in 1 BAG	PATCH	40		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84640-001	MUGWORT PATCH PATCH [YIWU QUYAN E-COMMERCE TRADING CO., LTD.]	1	1 package rows	20240815_1f8e2819-5a60-9114-e063-6394a90a3782.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Mugwort patch
ACONITUM CARMICHAELII ROOT
ARTEMISIA PRINCEPS LEAF
GINGER OIL
LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT
FRANKINCENSE
KAEMPFERIA GALANGA ROOT
ANGELICA DAHURICA ROOT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84640-001	84640-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ACONITUM CARMICHAELII ROOT	XJ28061U1S	IACT
ARTEMISIA PRINCEPS LEAF	SY077EW02G	ACTIB
GINGER OIL	SAS9Z1SVUK	IACT
LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT	RR83T99U97	IACT
FRANKINCENSE	R9XLF1R1WM	IACT
KAEMPFERIA GALANGA ROOT	7B7U9D12AI	IACT
ANGELICA DAHURICA ROOT	1V63N2S972	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
1f8e2819-5a61-9114-e063-6394a90a3782			1f8e2819-5a60-9114-e063-6394a90a3782	2024-08-13	Warnings	Exact identifier spl id: 1f8e2819-5a61-9114-e063-6394a90a3782 spl set id: 1f8e2819-5a60-9114-e063-6394a90a3782

Reported adverse events (FAERS/openFDA)#

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