MQXUNMI LIDOCAINE PAIN RELIEF PATCH- lidocaine pain relief patch patch

MQXUNMI LIDOCAINE Pain Relief Patch by

Drug Labeling and Warnings

MQXUNMI LIDOCAINE Pain Relief Patch by is a Otc medication manufactured, distributed, or labeled by Zhengzhou Miaoqi Medical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine 4%
Menthol 3%

Purpose

Topical Analgesic
wrist, knees, back, neck, hips, shoulders, elbows.

Use

For temporary relief of pain

Warnings

For external use only

Do not use

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 contact a Poison Control Center right away

When Using

When Using
use only as directed

█ avoid contact with the eyes, mucous membranes or rashes

█ do not bandage tightly

Stop Use

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.Chidren under 12 years of age:consult a doctor.

Ask Doctor

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.Chidren under 12 years of age:consult a doctor.

Keep Out Of Reach Of Children

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

Directions

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

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

Inactive ingredients

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

Questions

Email:MQXUNMI@gmail.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MQXUNMI LIDOCAINE PAIN RELIEF PATCH 
lidocaine pain relief patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83781-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	3 g  in 100
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100

Inactive Ingredients
Ingredient Name	Strength
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
GLYCERIN (UNII: PDC6A3C0OX)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
POVIDONE K90 (UNII: RDH86HJV5Z)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
METHYLPARABEN (UNII: A2I8C7HI9T)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
TARTARIC ACID (UNII: W4888I119H)
WATER (UNII: 059QF0KO0R)
KAOLIN (UNII: 24H4NWX5CO)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83781-015-01	10 in 1 BOX; Type 0: Not a Combination Product	01/28/2026
2	NDC: 83781-015-02	12 in 1 BOX; Type 0: Not a Combination Product	01/28/2026
3	NDC: 83781-015-03	15 in 1 BOX; Type 0: Not a Combination Product	01/28/2026
4	NDC: 83781-015-04	16 in 1 BOX; Type 0: Not a Combination Product	01/28/2026
5	NDC: 83781-015-05	36 in 1 BOX; Type 0: Not a Combination Product	01/28/2026
6	NDC: 83781-015-06	50 in 1 BOX; Type 0: Not a Combination Product	01/28/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/28/2026

Labeler - Zhengzhou Miaoqi Medical Technology Co., Ltd. (701762807)

Establishment
Name	Address	ID/FEI	Business Operations
Zhengzhou Miaoqi Medical Technology Co., Ltd.		701762807	manufacture(83781-015)