lidocaine pain relief patches

Manufacturer
Changsha Maocheng Trading Co., Ltd
Effective date
2025-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:08:44

Label at a glance#

Productlidocaine pain relief patches
Active ingredientMENTHOL, LIDOCAINE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1.8%

INACTIVE INGREDIENT SECTION

Purified water
g1 ycerol
Glucosamine
polyving akohol
Tartaric acid
Disodium edetate dihydrate
Aluminium glycinat
Sodium polyacrylate

OTC - PURPOSE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with:
msimple backache marthritis mstrains mbruises msprains

WARNINGS SECTION

WarningsFor external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets. lf swallowed, get medical help or contacta Poison Control Center(1-800-222-1222)right away.

INDICATIONS & USAGE SECTION

Directions
Adults and children 12 years of age and over: Clean and dry affected area,free of lotions, ointments and creams.Carefully remove backing starting at a corner.Apply sticky side of patch to affected area. Do not use more than onepatch in a 12 hourperiod. Repeat as necessary. Maximum 2 patches per day. Discard patch after singleuse.Children under 12 years of age: consult a physician.

DOSAGE & ADMINISTRATION SECTION

Maximum 2 patches per day. Discard patch after singleuse.Children under 12 years of age: consult a physician.

OTHER SAFETY INFORMATION

Otherinformation
Store in a clean, dry place outside of direct sunlight, Protect from excessive moisture.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

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
84876-101-01lidocaine pain relief patches6 in 1 BOXPATCH61
84876-101-01lidocaine pain relief patches10 g in 1 PATCHPATCH101

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84876-10184876-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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 patchesLIDOCAINEChangsha Maocheng Trading Co., Ltd3afeead3-4f5c-4711-e063-6294a90aacca2025-07-28WarningsExact identifier
ndc (package): 84876-101-01
ndc (product): 84876-101
ndc11 (package): 84876010101
spl id: 3afeead3-4f5d-4711-e063-6294a90aacca
spl set id: 3afeead3-4f5c-4711-e063-6294a90aacca

Reported adverse events (FAERS/openFDA)#

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