Label at a glance#

ProductMenthol Patch

Active ingredientMENTHOL

Label structure13 sections

Dosage and administration

Take one piece of this product when needed, remove the waxpaper, stick to the desired area and press the surrounding, replace it every 8 hours. Children should be used under adult supervision.

Storage and handling

Store the product in a cool, dry and well-ventilated place Avoid direct sunlight

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 19.0%

Purpose

OTC - PURPOSE SECTION

Pain Relief

Use

INDICATIONS & USAGE SECTION

Temporarily relieves muscle soreness and minor joints pain related to arthritis, backache, strains, sprains

Warnings

WARNINGS SECTION

For external use only. Do not take it internally.

Keep Out Of Reach Of Children
Sensitive Skin

Do not use

OTC - DO NOT USE SECTION

Product shall not be eat

When Using

OTC - WHEN USING SECTION

Use only as directedAvoid contacting with eyes or mucous membranesDo not apply to wounds or damaged skinDo not use with other ointments, creams, sprays, or linimentsDo not bandage or use with heating pad or devictStore in a cool dry place away from direct sunlight

Stop Use

OTC - STOP USE SECTION

In case of adverse reactions, please stop using this product.If the symptoms.

Ask Doctor

OTC - ASK DOCTOR SECTION

ask doctor in case of Sensitive Skin

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children

Directions

DOSAGE & ADMINISTRATION SECTION

Take one piece of this product when needed, remove the waxpaper,

stick to the desired area and press the surrounding, replace it every 8 hours.

Children should be used under adult supervision.

Other information

STORAGE AND HANDLING SECTION

Store the product in a cool, dry and well-ventilated place

Avoid direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

Far-infrared Nano Ceramic Powder,

Medical Adhesive Paste,

Backing

Silicone Oil Paper

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7fd951fe-040a-0b64-2bea-eefc6aa4fc54	Product name	2	20250515
5b0ed980-56ce-7dd0-fb86-ff54be67c2e6	Product name	2	20200925
eed31638-1288-4eb6-a55c-5fc014dca98d	Product name	3	20200728

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
83675-010-01	2025-01-30	C162847	48780-1	1030e365-304b-111a-e063-dadaa90a10e2	05c6a652-5e3c-6920-e063-6294a90adecf
83675-010-01	2024-01-30	C162847	48780-1	1030e365-304b-111a-e063-dadaa90a10e2	05c6a652-5e3c-6920-e063-6294a90adecf

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83675-010-01	Menthol Patch	8 in 1 BAG	PATCH	8		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83675-010	MENTHOL PATCH PATCH [GUANGZHOU HANHAI TRADING CO., LTD]	1	1 package rows	20230921_05c6a652-5e3c-6920-e063-6294a90adecf.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Menthol Patch
POWDERED CELLULOSE
IVERMECTIN
DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (40/60 W/W; 1000000 PA.S)
MENTHOL
BACKHOUSIA MYRTIFOLIA WHOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83675-010	83675-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POWDERED CELLULOSE	SMD1X3XO9M	IACT
IVERMECTIN	8883YP2R6D	IACT
DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (40/60 W/W; 1000000 PA.S)	83D19O7250	IACT
MENTHOL	L7T10EIP3A	ACTIB
BACKHOUSIA MYRTIFOLIA WHOLE	M5B93S0VJK	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
05c6a652-5e3d-6920-e063-6294a90adecf			05c6a652-5e3c-6920-e063-6294a90adecf	2023-09-20	Warnings	Exact identifier spl id: 05c6a652-5e3d-6920-e063-6294a90adecf spl set id: 05c6a652-5e3c-6920-e063-6294a90adecf

Reported adverse events (FAERS/openFDA)#

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