83781-016

Manufacturer
Zhengzhou Miaoqi Medical Technology Co., Ltd.
Effective date
2026-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:37:01

Label at a glance#

ProductMQ Lidocaine Pain Relief Patch
Active ingredientLIDOCAINE, MENTHOL
Label structure14 sections

Dosage and administration

PU film patch Adults and Children above 12 years old 1. Pinch the white side tab,and peel off the whole paper backing. 2.Peel off the transparent plastic film on the medicine layer. 3.Align the patch, gently place it, and press firmly. 4.From the blue center line, tear off the front protective film to the left and right. 5.Finally, remove the side tabs. Children under age of 12: Consult a doctor. Non-woven fabric ...

Storage and handling

Storage: Store in a clean, dry place outside of direct sunlight. Protect product from excessive moisture.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%
Menthol 3%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

use only as directed
avoid contact with the eyes, mucous membranes or rashes
do not bandage tightly

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

1. Not for use by pregnant or nursing women, infants, or anyone allergic to any ingredient.
2.Do not use on wounds or damaged skin.
3.Do not use with other patch,ointments,creams ,sprays,or liniments
4.Do not tightly wrap the application area or use local heat sources (such as heating pads) on it.
5.Do not use more than 1 patch at a time.
6.Avoid contact with the eyes.
7.Keep out of reach of children. If swallowed, get medical help or contactta Poison Control Center right away.

When Using

OTC - WHEN USING SECTION

use only as directed
avoid contact with the eyes, mucous membranes or rashes
do not bandage tightly

Stop Use

OTC - STOP USE SECTION

1.If you experience any signs of worsening or skin damage, such as redness, irritation, swelling, or blistering.
2.If symptoms persist for more than 7 days, or if symptoms clear up and then reappear within a few days.
3.If you are pregnant or breastfeeding, consult a healthcare professional before use.
4.Children under 12 years of age:consult a doctor.

Ask Doctor

OTC - ASK DOCTOR SECTION

1.If you experience any signs of worsening or skin damage, such as redness, irritation, swelling, or blistering.
2.If symptoms persist for more than 7 days, or if symptoms clear up and then reappear within a few days.
3.If you are pregnant or breastfeeding, consult a healthcare professional before use.
4.Children under 12 years of age:consult a doctor.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

PU film patch
Adults and Children above 12 years old
1. Pinch the white side tab,and peel off the whole paper backing.
2.Peel off the transparent plastic film on the medicine layer.
3.Align the patch, gently place it, and press firmly.
4.From the blue center line, tear off the front protective
film to the left and right.
5.Finally, remove the side tabs.
Children under age of 12: Consult a doctor.
Non-woven fabric patch
Adults and Children above 12 years old
1.Clean and dry the skin.
2.Prepare the adhesive secure patch and peel off its
backing.
3.Peel off the pain patch's protective film.
4.Apply to the target area.
5.Press to secure in place.
Children under age of 12: Consult a doctor.

Other information

STORAGE AND HANDLING SECTION

Storage: Store in a clean, dry place outside of direct sunlight. Protect product from excessive moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aluminum Glycinate,Edetate Disodium,Ethylhexylglycerin,Glycerin,Kaolin,Phenoxyethanol,Polyvinylpyrrolidone,Propylene Glycol,Sodium Carboxymethyl Cellulose,Sodium Polyacrylate,Tartaric Acid,Water

Questions

OTC - QUESTIONS SECTION

mqmq69002@gmail.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122334455668899

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136979861601517GTIN-13: 6979861601517
EAN-13: 6979861601517
GTIN storage (14 digits): 06979861601517
16.jpg

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MQ Lidocaine Pain Relief PatchLIDOCAINE PAIN RELIEF PATCHZhengzhou Miaoqi Medical Technology Co., Ltd.5560cdab-cee8-f6ec-e063-6294a90ad0242026-06-29WarningsExact identifier
ndc (package): 83781-016-07
ndc (package): 83781-016-06
ndc (package): 83781-016-08
ndc (package): 83781-016-01
ndc (package): 83781-016-03
ndc (package): 83781-016-04
ndc (package): 83781-016-02
ndc (package): 83781-016-05
ndc (product): 83781-016
ndc11 (package): 83781001607
ndc11 (package): 83781001603
ndc11 (package): 83781001606
ndc11 (package): 83781001605
ndc11 (package): 83781001602
ndc11 (package): 83781001608
ndc11 (package): 83781001604
ndc11 (package): 83781001601
spl id: 5560cdab-cee9-f6ec-e063-6294a90ad024
spl set id: 5560cdab-cee8-f6ec-e063-6294a90ad024

Reported adverse events (FAERS/openFDA)#

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