87518-185

Manufacturer
Guangzhou Sumi Technology Innovation Co., Ltd
Effective date
2026-05-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:57:19

Label at a glance#

ProductLidocaine Pain Relief Gel -Patch
Active ingredientLIDOCAINE
Label structure15 sections

Indications and uses

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

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 affected area. · Carefully remove remaining film while pressing the patch firmly on the skin. · Apply 1 patch at a time to affected area, not more than 3 to 4 times daily. · Remove patch from the skin after at most 8-hour application Children under age of 12:Consu...

Storage and handling

Store at 20°C to 25°C (68°F - 77°F) Store in a cool dry place away from direct sunlight

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4% ...... Purpose: Topical Anesthetic

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

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

· 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

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.

Ask a doctor if:

OTC - ASK DOCTOR SECTION

· localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering

· condition worsens

· symptoms persist for more than 7 days

· symptoms clear up and occur again within a few days

Stop use if:

OTC - STOP USE SECTION

· localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering

· condition worsens

· symptoms persist for more than 7 days

· symptoms clear up and occur again within a few days

Pregnancy or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed accidentally , get medical help or contact with Poison Control Center immediately.

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 affected area.

· Carefully remove remaining film while pressing the patch firmly on the skin.

· Apply 1 patch at a time to affected area, not more than 3 to 4 times daily.

· Remove patch from the skin after at most 8-hour application

Children under age of 12:Consult a doctor

Other information

STORAGE AND HANDLING SECTION

Store at 20°C to 25°C (68°F - 77°F)

Store in a cool dry place away from direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Kaolin, Methylparaben, Polysorbate 80, PropyleneGlycol, Polyacrylic Acid, Povidone, Propylparaben, Sodium Polyacrylate, Titanium Dioxide, Tartaric Acid, Water

Questions or Comments?

OTC - QUESTIONS SECTION

supports@povihomeofficial.com

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

patchpatch9 patches9 patches12 patches12 patches15 patches15 patches

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1737778lidocaine 4 % Medicated PatchPSN2
1737778lidocaine 0.04 MG/MG Medicated PatchSCD2
1737778lidocaine 4 % Medicated PatchSY2

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-136942488032552GTIN-13: 6942488032552
EAN-13: 6942488032552
GTIN storage (14 digits): 06942488032552
9_patch.jpg
BarcodeEAN-136942488032569GTIN-13: 6942488032569
EAN-13: 6942488032569
GTIN storage (14 digits): 06942488032569
12_patch.jpg
BarcodeEAN-136942488032576GTIN-13: 6942488032576
EAN-13: 6942488032576
GTIN storage (14 digits): 06942488032576
15_patch.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
87518-185-09Lidocaine Pain Relief Gel -Patch9 in 1 BOXPATCH92
87518-185-09Lidocaine Pain Relief Gel -Patch1 in 1 BAGPATCH12
87518-185-12Lidocaine Pain Relief Gel -Patch1 in 1 BAGPATCH12
87518-185-12Lidocaine Pain Relief Gel -Patch12 in 1 BOXPATCH122
87518-185-15Lidocaine Pain Relief Gel -Patch15 in 1 BOXPATCH152
87518-185-15Lidocaine Pain Relief Gel -Patch1 in 1 BAGPATCH12

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87518-18587518-185-12, 87518-185-15, 87518-185-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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 Gel -PatchLIDOCAINEGuangzhou Sumi Technology Innovation Co., Ltd514900f1-7fcb-636a-e063-6394a90a4ba22026-05-14WarningsExact identifier
ndc (package): 87518-185-12
ndc (package): 87518-185-15
ndc (package): 87518-185-09
ndc (product): 87518-185
ndc11 (package): 87518018512
ndc11 (package): 87518018509
ndc11 (package): 87518018515
spl id: 51c4fb44-a073-1305-e063-6294a90af88e
spl set id: 514900f1-7fcb-636a-e063-6394a90a4ba2

Reported adverse events (FAERS/openFDA)#

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