Foot Pain Relief Gel-Patch 15;22;30

Manufacturer
Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
Effective date
2026-08-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-18 02:03:17

Label at a glance#

ProductFoot Pain Relief Gel-Patch
Active ingredientMENTHOL, LIDOCAINE
Label structure13 sections

Indications and uses

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

Dosage and administration

Adult and Children above12 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. Apply 1 patch at a time to affected area, not morethan 3 to 4 times daily. Remove patch from the skin after at most 8-hour application Children under 12 years of age: Consult a do...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

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

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

Purposes

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, neck, shoulders, elbows.

Warnings

WARNINGS SECTION

For external use only

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
  • dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

Do not use:

OTC - DO NOT USE SECTION

  • more than 1 patch on your body at a time or with other topical anesthetics at the same time
  • 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

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering
  • condition worsen
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few 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, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adult and Children above12 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.
  • Apply 1 patch at a time to affected area, not morethan 3 to 4 times daily.
  • Remove patch from the skin after at most 8-hour application

Children under 12 years of age:Consult a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Dihydroxyaluminium Aminoacetate, Edetate Disodium, Glycerin, Hydroxyacetophenone,Kaolin, L(+)-Tartaric Acid, Mineral oil, Polysorbate80, Polyacrylic Acid , Polyvinylpyrrolidone K90,Propylene Glycol, Sodium Polyacrylate,

Titanium Dioxide, Water.

Questions or Comments

OTC - QUESTIONS SECTION

supports@sumifunofficialcom

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

174-09174-09174-10174-10patchpatch151522223030

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136942488008137GTIN-13: 6942488008137
EAN-13: 6942488008137
GTIN storage (14 digits): 06942488008137
174-15.jpg
BarcodeEAN-136942488008144GTIN-13: 6942488008144
EAN-13: 6942488008144
GTIN storage (14 digits): 06942488008144
174-22.jpg
BarcodeEAN-136942488008151GTIN-13: 6942488008151
EAN-13: 6942488008151
GTIN storage (14 digits): 06942488008151
174-30.jpg
BarcodeEAN-136942488054851GTIN-13: 6942488054851
EAN-13: 6942488054851
GTIN storage (14 digits): 06942488054851
10patches.jpg
BarcodeEAN-136942488054868GTIN-13: 6942488054868
EAN-13: 6942488054868
GTIN storage (14 digits): 06942488054868
9patches.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

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
83602-17483602-174-01, 83602-174-15, 83602-174-22, 83602-174-30, 83602-174-09, 83602-174-10

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-05-14full-release2026-06-01 01:57:30
12026-01-24monthly-update2026-06-03 17:53:10

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
Foot Pain Relief Gel-PatchLIDOCAINE AND MENTHOLGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.49220240-5410-eb6d-e063-6394a90a13282026-08-14WarningsExact identifier
ndc (package): 83602-174-09
ndc (package): 83602-174-22
ndc (package): 83602-174-10
ndc (package): 83602-174-01
ndc (package): 83602-174-30
ndc (package): 83602-174-15
ndc (product): 83602-174
ndc11 (package): 83602017430
ndc11 (package): 83602017415
ndc11 (package): 83602017410
ndc11 (package): 83602017409
ndc11 (package): 83602017401
ndc11 (package): 83602017422
spl id: 58fe5428-93dc-6c14-e063-6294a90abd3c
spl set id: 49220240-5410-eb6d-e063-6394a90a1328

Reported adverse events (FAERS/openFDA)#

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