Lidocaine Pain Relief Patch

Manufacturer
Henan Shouerkang Health Industry Co., Ltd
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:31:40

Label at a glance#

ProductLidocaine Pain Relief Patch
Active ingredientMENTHOL, LIDOCAINE
Label structure12 sections

Dosage and administration

Adults and children above 12 years old; Clean and dry the affected area. Tear off the protective film and apply the exposed part of the patch to the the affected area. Carefully remove remaining film while pressing the patch firmly on the skin. Remove patch from the skin after at most 8 hours application. Children under age of 12:C onsult a doctor

Storage and handling

No Data

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic
Pain Relief

Use

INDICATIONS & USAGE SECTION

Temporarily relieves muscle soreness and minor joint pains
in the wrist, knees, back, neck, hips, shoulders, elbows.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on wounds or damaged skin with a heating pad or device with other ointments, creams, sprays, or liniments
if your are allergic to any ingredients of this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

if skin reactions such as redness, swelling, blistering or other discomfort occur symptoms persist for more than 7 days
If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children.
If swallowed accidentally , get medical help or contact with Poison Control Center immediately

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children above 12 years old;
Clean and dry the affected area.
Tear off the protective film and apply the exposed part of the patch to the the affected area.
Carefully remove remaining film while pressing the patch firmly on the skin.
Remove patch from the skin after at most 8 hours application.
Children under age of 12:C onsult a doctor

Other information

STORAGE AND HANDLING SECTION

No Data

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerine、Alcohol、 Aluminium glycinate、Sodium Polyacrylate、Pvpk-90、
Tartaric acid Propylparaben、 Methylparaben、 Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85056-001-01Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-02Lidocaine Pain Relief Patch8 in 1 BOXPASTE82
85056-001-03Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-04Lidocaine Pain Relief Patch10 in 1 BOXPASTE102
85056-001-05Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-06Lidocaine Pain Relief Patch12 in 1 BOXPASTE122
85056-001-07Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-08Lidocaine Pain Relief Patch15 in 1 BOXPASTE152
85056-001-09Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-10Lidocaine Pain Relief Patch16 in 1 BOXPASTE162
85056-001-11Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-12Lidocaine Pain Relief Patch18 in 1 BOXPASTE182
85056-001-13Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-14Lidocaine Pain Relief Patch20 in 1 BOXPASTE202
85056-001-15Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-16Lidocaine Pain Relief Patch25 in 1 BOXPASTE252
85056-001-17Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-18Lidocaine Pain Relief Patch28 in 1 BOXPASTE282
85056-001-19Lidocaine Pain Relief Patch1 in 1 BAGPASTE12
85056-001-20Lidocaine Pain Relief Patch32 in 1 BOXPASTE322

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
Lidocaine Pain Relief PatchLIDOCAINE PAIN RELIEF PATCHHenan Shouerkang Health Industry Co., Ltd29aefb41-bf5b-1c3c-e063-6294a90a95702026-01-07WarningsExact identifier
ndc (package): 85056-001-08
ndc (package): 85056-001-15
ndc (package): 85056-001-05
ndc (package): 85056-001-01
ndc (package): 85056-001-14
ndc (package): 85056-001-09
ndc (package): 85056-001-16
ndc (package): 85056-001-03
ndc (package): 85056-001-10
ndc (package): 85056-001-12
ndc (package): 85056-001-17
ndc (package): 85056-001-07
ndc (package): 85056-001-06
ndc (package): 85056-001-02
ndc (package): 85056-001-18
ndc (package): 85056-001-11
ndc (package): 85056-001-13
ndc (package): 85056-001-04
ndc (package): 85056-001-20
ndc (package): 85056-001-19
ndc (product): 85056-001
ndc11 (package): 85056000113
ndc11 (package): 85056000110
ndc11 (package): 85056000115
ndc11 (package): 85056000104
ndc11 (package): 85056000119
ndc11 (package): 85056000101
ndc11 (package): 85056000117
ndc11 (package): 85056000102
ndc11 (package): 85056000106
ndc11 (package): 85056000103
ndc11 (package): 85056000109
ndc11 (package): 85056000111
ndc11 (package): 85056000108
ndc11 (package): 85056000107
ndc11 (package): 85056000116
ndc11 (package): 85056000120
ndc11 (package): 85056000112
ndc11 (package): 85056000118
ndc11 (package): 85056000114
ndc11 (package): 85056000105
spl id: 47c8aec2-4691-76a3-e063-6294a90a45fd
spl set id: 29aefb41-bf5b-1c3c-e063-6294a90a9570

Reported adverse events (FAERS/openFDA)#

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