Mugwort

Manufacturer: Henan Toudaorong Biotechnology Co., Ltd.
Effective date: 2025-01-19
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:53:18

Label at a glance#

ProductMugwort

Active ingredientPEPPERMINT, CAMPHOR (NATURAL)

Label structure10 sections

Label contents#

Full prescribing information#

Active ingredients (Strength)

OTC - ACTIVE INGREDIENT SECTION

Peppermint 3g/100g Camphor 0.5g/100g

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients

Mugwort Leaf Extract, Peppermint Leaf Oil, Curcuma longa, Cinnamon Extract,Safflower Extract, Camphor

Purpose

OTC - PURPOSE SECTION

Promote blood circulation

Relieve muscle soreness

Soothe joint discomfort

Relieve cold and dampness

OTC - keep out of reach of children section

Adults only.

Indications & usage section

Indications for Use:

· Relieve Pain.

· Improve Blood Circulation

· Reduce Inflammation.

· Support Joint Mobility.

· Soothing Effect

Warnings section

lf symptoms persist, please consult your healthcare professionals. Non-GMO/Gluten Free.This product cannot replace medicine. Allergens, pregnant women, and children are prohibited from using it.

Dosage & administration section

1. Do not apply on areas with skin redness, swelling, congestion, ulceration, or damage.

2. Not suitable for individuals with allergic tendencies.

3. Pregnant women, and children are prohibited from using it.

4. A small number of people may experience local itching or red rash during use, which is not harmful. Symptoms will gradually disappear after stopping use.

5. Skin burning sensation during use is a normal phenomenon.

6. This product is a daily household item and cannot replace medicine or medical equipment.

If discomfort occurs, stop using the product. If necessary, consult a doctor.

OTC - STOP USE SECTION

lf symptoms persist, please consult your healthcare professionals. Non-GMO/Gluten Free.This product cannot replace medicine. Allergens, pregnant women, and children are prohibited from using it.

when

OTC - WHEN USING SECTION

1. Do not apply on areas with skin redness, swelling, congestion, ulceration, or damage.

2. Not suitable for individuals with allergic tendencies.

3. Pregnant women, and children are prohibited from using it.

4. A small number of people may experience local itching or red rash during use, which is not harmful. Symptoms will gradually disappear after stopping use.

5. Skin burning sensation during use is a normal phenomenon.

6. This product is a daily household item and cannot replace medicine or medical equipment.

If discomfort occurs, stop using the product. If necessary, consult a doctor.

package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mugwort Patch

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
PEPPERMINT Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85136-001-01	Mugwort	7 in 1 BOX	PATCH	7		1
85136-001-01	Mugwort	10 g in 1 PATCH	PATCH	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
85136-001	MUGWORT PATCH [HENAN TOUDAORONG BIOTECHNOLOGY CO., LTD.]	1	2 package rows	20250122_2c1173b1-b339-9e76-e063-6394a90ac923.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Mugwort
CINNAMON OIL
PEPPERMINT
SAFFLOWER
CAMPHOR (NATURAL)
ARTEMISIA PRINCEPS LEAF
CURCUMA LONGA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85136-001	85136-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CINNAMON OIL	E5GY4I6YCZ	IACT
PEPPERMINT	V95R5KMY2B	ACTIB
SAFFLOWER	4VBL71TY4Y	IACT
CAMPHOR (NATURAL)	N20HL7Q941	ACTIB
ARTEMISIA PRINCEPS LEAF	SY077EW02G	IACT
CURCUMA LONGA LEAF	H2HC4RY52C	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
2c1173b1-b33a-9e76-e063-6394a90ac923			2c1173b1-b339-9e76-e063-6394a90ac923	2025-01-19	Warnings	Exact identifier spl id: 2c1173b1-b33a-9e76-e063-6394a90ac923 spl set id: 2c1173b1-b339-9e76-e063-6394a90ac923

Reported adverse events (FAERS/openFDA)#

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