Lidocaine Pain Relief Gel-Patch

Manufacturer
Shenzhen Wankelai E-commerce Co., Ltd.
Effective date
2026-02-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:37:12

Label at a glance#

ProductLidocaine Pain Relief Gel-Patch
Active ingredientLIDOCAINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

OTC - PURPOSE SECTION

Topical Anesthetic

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION


More than one patch on your body at a time.
On wounds or damaged skin.
On puncture wounds.
For more than one week without consulting a doctore
lf pouch is damaged or opened.
lf your are allergic to any ingredients of this product.

OTC - WHEN USING SECTION


Use only as directede
Read and follow all directions and warnings on this carton
Do not allow contact with the eyes
Do not use at the same time as other topical analgesicse
Do not bandage tightly or apply local heat (such asheating pads) to the area of use
Do not microwave
Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that canproduce serious adverse effects if a child or pet chews or ingests this patch.

OTC - STOP USE SECTION


Condition worsens
Redness is present
lrritation develops
Symptoms persist for more than 7 days or clear up andoccur again within a few days
You experience signs of skin injury, such as pain,swelling or blistering where the product was applied.
Ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


If swallowed, get medical help or contact a Poison
Control Center right away.

DOSAGE & ADMINISTRATION SECTION


Adults and children 12 years of age and over:
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.Patch firmly on the skin.
Remove patch from the skin after at most 8-hour application.
Discard the patch after a single use.
Children under 12 years of age: consult a physician.

INACTIVE INGREDIENT SECTION

Aluminum Glycinate, Aluminum Hydroxide, Cellulose Gum
DMDM hydantoin,Glycerin, Polyacrylic Acid
Polysorbate 80, Propylene Glycol, Ricinus Communis Seed Oil (castor)
Silica, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Urea, Water, Menthol
Aloe Vera, Vitamin E

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1737778lidocaine 4 % Medicated PatchPSN1
1737778lidocaine 0.04 MG/MG Medicated PatchSCD1
1737778lidocaine 4 % Medicated PatchSY1

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
87413-001-01Lidocaine Pain Relief Gel-Patch32 in 1 BOXPATCH321
87413-001-01Lidocaine Pain Relief Gel-Patch1 in 1 PATCHPATCH11

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87413-00187413-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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-PatchLIDOCAINEShenzhen Wankelai E-commerce Co., Ltd.4a22562b-601e-97d7-e063-6394a90a5bca2026-02-06WarningsExact identifier
ndc (package): 87413-001-01
ndc (product): 87413-001
ndc11 (package): 87413000101
spl id: 4a22562b-601f-97d7-e063-6394a90a5bca
spl set id: 4a22562b-601e-97d7-e063-6394a90a5bca

Reported adverse events (FAERS/openFDA)#

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