4% Lidocaine Patch

Manufacturer
Hengyang Chuangjiujia Trading Co., Ltd.
Effective date
2025-11-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:42:20

Label at a glance#

Product4% Lidocaine Patch
Active ingredientLIDOCAINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

OTC - PURPOSE SECTION

Topical Aneslhetic

INDICATIONS & USAGE SECTION

Use Temperarily relicwes miner pain.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use More than one patch on your body at a time On gut, initated orswollen gkin On puncture wounds For more than one week without consultinga doctor if you are allergic to any aclive or inactive ingrediantsm lf pouch iscambged or opred.

OTC - WHEN USING SECTION

When using this product Use only as directed Read and follow all directionsand warings on this carton Do not allow oontact with the oyes Do not use atthe same lime as oler bopical analgesics Do nat bandage lighlly or apoly localheat (such as heating pads, to the area of use Dispose of uged patch inmannerihat always keeps product away irom children and pots, Lised paiches siilcontain the drug product that can produce gerious adverge elfecis if a child or petchaws or ingasis ihis patchh.

OTC - STOP USE SECTION

Stop use and consult a doctor if condtion worsensm Redness is presert lniation develops Sympioms persist for more than 7 dlays or clear up and oocuragain willin a ferw darys You coperienoe signs of skin injury, such as pain, sweling or bllslering where the product was applled.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

DOSAGE & ADMINISTRATION SECTION

Adults and chldren 12 years of age and over: Clean and dry affected areaCarefully remove backing from patchstarting at a corner. Apply sticky sideof patch to affected area. Use one patch for up to 12 hours. Discard patchaftersingle use. Children under 12 years of age: consult a physician.

INACTIVE INGREDIENT SECTION

Aluminum Glycinate
Aluminum Hydroxide
Cellulose Gum (Sodium CMC)
DMDM Hydantoin
Glycerin
Polyacrylic Acid
Polysorbate 80
Propylene Glycol
Ricinus Communis (Castor) Seed Oil
Silica (Colloidal)
Sodium Polyacrylate
Tartaric Acid
Titanium Dioxide
Urea
Water (Purified Water)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1737778lidocaine 4 % Medicated PatchPSN3
1737778lidocaine 0.04 MG/MG Medicated PatchSCD3
1737778lidocaine 4 % 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
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
84735-010-014% Lidocaine Patch20 in 1 BOXPATCH203

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84735-01084735-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-05-21full-release2026-06-01 01:01:28

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
42e8ff2d-7db7-49f1-e063-6394a90ad85e35a15e60-b33c-5065-e063-6294a90ad9df2025-11-06WarningsExact identifier
spl id: 42e8ff2d-7db7-49f1-e063-6394a90ad85e
spl set id: 35a15e60-b33c-5065-e063-6294a90ad9df

Reported adverse events (FAERS/openFDA)#

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