LIDOCAINE PAIN RELIEVING GEL-PATCH- lidocaine patch

Lidocaine Pain Relieving Gel-Patch by

Drug Labeling and Warnings

Lidocaine Pain Relieving Gel-Patch by is a Otc medication manufactured, distributed, or labeled by Nanjing Anxing Medical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine 4%

PURPOSE

Topical anesthetic

INDICATIONS & USAGE

Temporarily relieves minor pain
associated with:
arthritis
simple backache
muscle strains
sprains
bruises

WARNINGS

For external use only

DO NOT USE

on wounds or damaged, broken or irritated skin
with a heating pad
if you are allergic to any ingredients of this product

WHEN USING

Use only as directed
Do not bandage tightly
Avoid contact with eyes and mucous membranes
Temporary burning or redness at application site may occur
Rare cases of serlous burns have been reported with products of this type

STOP USE

condition worsens or symptoms persist for more than 7 days
symptoms clear up and occur again within a few days
severe burning sensation, itching, rash or skin irritation develops
If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Used patches contain a large amount of lidocaine. lf swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).Accidental exposure in children can result in death.

DOSAGE & ADMINISTRATION

Adults and children 12 years of age and over:
clean and dry affected area
remove film from patch and apply to the skin
apply one patch at a time to affected area
use 1 patch for up to 8 hours
do not use more than 3 to 4 times daily
Children under 12 years of age: consult
a doctor

INACTIVE INGREDIENT

WATER
POLYVINYL ALCOHOL
PHENOXYETHANOL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIDOCAINE PAIN RELIEVING GEL-PATCH 
lidocaine patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87125-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	0.04 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYVINYL ALCOHOL (UNII: 532B59J990)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87125-001-01	18 in 1 BOX	10/10/2025
1		1 in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 87125-001-02	36 in 1 BOX	10/10/2025
2		1 in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/10/2025

Labeler - Nanjing Anxing Medical Technology Co., Ltd. (711551921)

Establishment
Name	Address	ID/FEI	Business Operations
Nanjing Anxing Medical Technology Co., Ltd.		711551921	manufacture(87125-001)