FDA.reportPublic FDA data

Lidopatch

Manufacturer
Wuhan Bingbing Pharmaceutical Co., Ltd | Wuhan Bingbing Pharmaceutical Co., Ltd.
Effective date
2019-01-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:58:22

Label at a glance#

ProductLidopatch
Active ingredientLIDOCAINE, MENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

WARNINGS SECTION
For external use only. Do not use if you are allergic or sensitive to lidocaine or menhol. Do not use if pouch is damaged or opened.

OTC - PURPOSE SECTION

PURPOSE

Temporarily relieves minor pain associated with: arthritis, simple backache, bursitis, tendonitis, muscle straints, sprains and bruises.

OTC - ACTIVE INGREDIENT SECTION


ACTIVE INGREDIENT SECTION
Lidocaine HCL 3.6% - Topical analgesic
Menthol 1.25% - Topical analgesic

OTC - STOP USE SECTION

STOP USE SECTION
Stop Use and ask doctor if:
excessive redness or irritation is present
Pain persists for more than 7 days
symptoms cear up and occur again within a few days
conditions worsens
If pregnant or breasfeading, ask a health professional before use. keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION SECTION


Directions: Aduts apply patch to affected area for a maximum of 12 hours.
Do not use more than 1 patch every 24 hours.
children : consult your physician
remove protective film, gently apply to affected area.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION


Aloe Barbadensis, Diazolidinyl Urea, EDTA Disodium Salt, Glycerin, Iodpropynyl, Butylcarbonate, Methylparaben, Polysorbate 80, Propylparaben, Sodium Polyacrylate, Water

INDICATIONS & USAGE SECTION

Usage
Aduts apply patch to affected area for a maximum of 12 hours.
Do not use more than 1 patch every 24 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LidopatchLidopatch

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1792852lidocaine 3.6 % / menthol 1.25 % Medicated PatchPSN3
1739875LidoPatch 3.6 % / 1.25 % Medicated PatchPSN3
1739875lidocaine 0.036 MG/MG / menthol 0.0125 MG/MG Medicated Patch [Lidopatch]SBD3
1792852lidocaine 0.036 MG/MG / menthol 0.0125 MG/MG Medicated PatchSCD3
1792852lidocaine 3.6 % / menthol 1.25 % Medicated PatchSY3
1739875LidoPatch (lidocaine 3.6 % / menthol 1.25 % ) Medicated PatchSY3

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
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
70267-001-012021-01-29C16284748780-1ba0f9c33-2530-a910-e053-dadaa90a0b85Lidopatch
70267-001-022021-01-29C16284748780-1ba0f9c33-2530-a910-e053-dadaa90a0b85Lidopatch
70267-001-032021-01-29C16284748780-1ba0f9c33-2530-a910-e053-dadaa90a0b85Lidopatch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70267-001-01Lidopatch30 in 1 PACKAGEPATCH303
70267-001-02Lidopatch1 in 1 PACKAGEPATCH13
70267-001-03Lidopatch30 in 1 PACKAGEPATCH303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70267-001LIDOPATCH (LIDOCAINE, MENTHOL) PATCH [WUHAN BINGBING PHARMACEUTICAL CO., LTD]3Legacy NDC, 3 package rows20190130_29c762c0-4bbc-649b-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70267-00170267-001-02, 70267-001-01, 70267-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
LIDOCAINE98PI200987ACTIB
MENTHOLL7T10EIP3AACTIB
COBALT DISODIUM EDETATE3EY1Y2QRLIIACT
GLYCERINPDC6A3C0OXIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
POLYSORBATE 806OZP39ZG8HIACT
PROPYLPARABENZ8IX2SC1OHIACT
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
WATER059QF0KO0RIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
ALOE VERA LEAFZY81Z83H0XIACT
METHYLPARABENA2I8C7HI9TIACT

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
8088aed3-53b1-0d16-e053-2a91aa0a3a0429c762c0-4bbc-649b-e054-00144ff8d46c2019-01-28WarningsExact identifier
spl id: 8088aed3-53b1-0d16-e053-2a91aa0a3a04
spl set id: 29c762c0-4bbc-649b-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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