FDA.reportPublic FDA data

Pain Relief Gel-Patch

Manufacturer
Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
Effective date
2026-05-17
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:57:47

Label at a glance#

ProductPain Relief Gel-Patch
Active ingredientLIDOCAINE, MENTHOL
Label structure18 sections

Indications and uses

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

Dosage and administration

Adult 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 affected area. Carefully remove remaining film while pressing the patch firmly on the skin. Remove patch from the skin after at most 8-hour application. Children under age of 12: Consult a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4% ...... Purpose: Topical anesthetic

Menthol 1% ...... Purpose: Topical analgesic

Purpose

OTC - PURPOSE SECTION

Topical anesthetic (Lidocaine)

Topical analgesic (Menthol)

Uses

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 you are allergic to any ingredients of this product

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • skin reactions such as redness, swelling, blistering or other discomfort occur
  • symptoms persist for more than 7 days

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed accidentally, get medical help or contact with Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adult 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 affected area.
  • Carefully remove remaining film while pressing the patch firmly on the skin.
  • Remove patch from the skin after at most 8-hour application.

Children under age of 12:Consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Dihydroxyaluminium Aminoacetate, Edetate Disodium, Glycerin, Hydroxyacetophenone, Kaolin, L(+)-Tartaric Acid, Mineral oil, Polysorbate 80, Polyacrylic Acid, Polyvinylpyrrolidone K90, Propylene Glycol, Sodium Polyacrylate, Titanium Dioxide, Water.

Questions or Comments:

OTC - QUESTIONS SECTION

supports@sumifunofficial.com

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

patchpatch

172-18

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

172-18172-18

172-25

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

172-25172-25

172-31

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

172-31172-31

172-15

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1515

172-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

172-01172-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1249758lidocaine 4 % / menthol 1 % Medicated PatchPSN6
1249758lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated PatchSCD6
1249758lidocaine 4 % / menthol 1 % Medicated PatchSY6

DailyMed Pharmacologic Classes#

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974817677899GTIN-13: 6974817677899
EAN-13: 6974817677899
GTIN storage (14 digits): 06974817677899		172-01.jpg
BarcodeEAN-136977314349139GTIN-13: 6977314349139
EAN-13: 6977314349139
GTIN storage (14 digits): 06977314349139		172-18.jpg
BarcodeEAN-136977314349146GTIN-13: 6977314349146
EAN-13: 6977314349146
GTIN storage (14 digits): 06977314349146		172-25.jpg
BarcodeEAN-136977314349153GTIN-13: 6977314349153
EAN-13: 6977314349153
GTIN storage (14 digits): 06977314349153		172-31.jpg

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
83602-172-01Pain Relief Gel-Patch12 g in 1 PATCHPATCH126
83602-172-15Pain Relief Gel-Patch12 g in 1 PATCHPATCH126
83602-172-15Pain Relief Gel-Patch15 in 1 BOXPATCH156
83602-172-18Pain Relief Gel-Patch12 g in 1 PATCHPATCH126
83602-172-18Pain Relief Gel-Patch18 in 1 BOXPATCH186
83602-172-25Pain Relief Gel-Patch25 in 1 BOXPATCH256
83602-172-25Pain Relief Gel-Patch12 g in 1 PATCHPATCH126
83602-172-31Pain Relief Gel-Patch12 g in 1 PATCHPATCH126
83602-172-31Pain Relief Gel-Patch31 in 1 BOXPATCH316

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83602-17283602-172-15, 83602-172-18, 83602-172-25, 83602-172-31, 83602-172-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
LIDOCAINE98PI200987ACTIB
KAOLIN24H4NWX5COIACT
TARTARIC ACIDW4888I119HIACT
WATER059QF0KO0RIACT
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS1K713C615KIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POLYACRYLIC ACID (250000 MW)9G2MAD7J6WIACT
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
MINERAL OILT5L8T28FGPIACT
POLYSORBATE 806OZP39ZG8HIACT
GLYCERINPDC6A3C0OXIACT
EDETATE DISODIUM7FLD91C86KIACT
POVIDONE K90RDH86HJV5ZIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
MENTHOLL7T10EIP3AACTIB

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pain Relief Gel-PatchLIDOCAINE AND MENTHOLGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.0ae6cfd1-bbea-3fe6-e063-6294a90a541f2026-05-17WarningsExact identifier
ndc (package): 83602-172-25
ndc (package): 83602-172-31
ndc (package): 83602-172-18
ndc (package): 83602-172-15
ndc (package): 83602-172-01
ndc (product): 83602-172
ndc11 (package): 83602017231
ndc11 (package): 83602017218
ndc11 (package): 83602017215
ndc11 (package): 83602017201
ndc11 (package): 83602017225
spl id: 520ee72b-610c-3668-e063-6394a90a4499
spl set id: 0ae6cfd1-bbea-3fe6-e063-6294a90a541f
Pain Relief Gel-PatchLIDOCAINE AND MENTHOLGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.32e1df3a-2f8f-68df-e063-6294a90aa1d12026-05-17WarningsExact identifier
ndc (product): 83602-172

Reported adverse events (FAERS/openFDA)#

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