FDA.reportPublic FDA data

Lidocaine Pain Relief Gel-Patch

Manufacturer
Dongguan Haiyi Technology Co.,Ltd.
Effective date
2024-11-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:33:47

Label at a glance#

ProductLidocaine Pain Relief Gel-Patch
Active ingredientLIDOCAINE
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Sodium Polyacrylate,Dihydroxyaluminum Aminoacetate,Disodium EthylenediaminetetraaceticAcid, Kaolin, Titanium Dioxide,Poly-sorbate 80, Propylene Glycol, TartaricAcid, Polyacrylic Acid,Polyvinylpyrroli-done K90, Methylparaben,Propylpara-ben, Water.

Purpose section

OTC - PURPOSE SECTION

Desensitizes AggravatedNerves And Relieves Pain :

No lrritation

Stay-put Flexible Patch

Numbs Pain Away

Warning

WARNINGS SECTION

For external use only

stop use

OTC - STOP USE SECTION

on wounds or damaged skin

with a heating pad or devic

with other ointments, creams,sprays, or liniments

if your are allergic to any ingredients of this product

not use

OTC - DO NOT USE SECTION

Not suitable for use by children, pregnantor breast feeding people.

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.

HOW TO USE

INDICATIONS & USAGE SECTION

Adults and Children above 12 year sold:
Clean and dry the affected area.

Tear off the protective film andapply the exposed part of the patch tothe affected area.

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

Remove patch from the skin afterat most 8-hour application

Dosage

DOSAGE & ADMINISTRATION SECTION

take an appropriateamount,Use 2-3 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84732-082-012025-07-29C16284748780-13b156c62-2ffe-fb37-e063-e6dba90a4e072611c2c5-dfb1-9ccd-e063-6394a90a1ee9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84732-082-01Lidocaine Pain Relief Gel-Patch70 g in 1 BOXPATCH701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84732-082LIDOCAINE PAIN RELIEF GEL-PATCH PATCH [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]11 package rows20241105_2611c2c5-dfb1-9ccd-e063-6394a90a1ee9.zip

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
84732-08284732-082-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
DIHYDROXYALUMINUM AMINOACETATEDO250MG0W6IACT
PROPYLPARABENZ8IX2SC1OHIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
GLYCERINPDC6A3C0OXIACT
TARTARIC ACIDW4888I119HIACT
POLYACRYLIC ACID (250000 MW)9G2MAD7J6WIACT
POVIDONE K90RDH86HJV5ZIACT
METHYLPARABENA2I8C7HI9TIACT
MAGNESIUM DISODIUM EDTANDT563S5VZIACT
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
KAOLIN24H4NWX5COIACT
WATER059QF0KO0RIACT
POLYSORBATE 806OZP39ZG8HIACT
LIDOCAINE98PI200987ACTIB

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
2611c2c5-dfb2-9ccd-e063-6394a90a1ee92611c2c5-dfb1-9ccd-e063-6394a90a1ee92024-11-04WarningsExact identifier
spl id: 2611c2c5-dfb2-9ccd-e063-6394a90a1ee9
spl set id: 2611c2c5-dfb1-9ccd-e063-6394a90a1ee9

Reported adverse events (FAERS/openFDA)#

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