87278-003 4% Lidocaine Pain Relief Patch

Manufacturer
Guangxi Keyun E-commerce Co., Ltd.
Effective date
2026-07-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-07-21 05:10:20

Label at a glance#

Product4% Lidocaine Pain Relief 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

For temporary relief of pain

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION


more than 1 patch at a time
on wounds or damaged skin
with a heating pad
if you are allergic to any ingredients of this product

OTC - WHEN USING SECTION


use only as directed
avoid contact with the eyes,mucous membranes or rashes
do not bandage tightly

OTC - STOP USE SECTION


localized skin reactions occur,such as rash,itching,redness,irritation, pain,swelling and blistering
condition worsen
symptoms persist for more than 7 days
symptoms clear up and occur again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION


Adult and children 12 years of age and over:
clean and dry affected area
remove film from patch and apply to the skin (see illustration)
apply 1 patch at a time to affected area, not more than 3 to 4 times daily
remove patch from the skin after at most 8-hour application
Children under 12 years of age: consult a doctor

INACTIVE INGREDIENT SECTION

Glycerin
Dihydroxyaluminum aminoacetate anhydrous
Edetate disodium
Tartaric acid
Povidone K90
DMDM Hydantoin
Polysorbate 80
Propylene glycol
Carboxymethylcellulose sodium
Kaolin
Carbomer
Sodium polyacrylate
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
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1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

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
87278-00387278-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-06-22monthly-update2026-07-17 21:35:15
22026-04-13full-release2026-06-01 01:53:31
12026-01-29monthly-update2026-06-03 17:53:25

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
4% Lidocaine Pain Relief PatchLIDOCAINE 4%Guangxi Keyun E-commerce Co., Ltd.4981e9c3-2a19-aed8-e063-6294a90af2162026-07-17WarningsExact identifier
ndc (package): 87278-003-01
ndc (product): 87278-003
ndc11 (package): 87278000301
spl id: 56ca91ff-b620-10cb-e063-6294a90a608b
spl set id: 4981e9c3-2a19-aed8-e063-6294a90af216

Reported adverse events (FAERS/openFDA)#

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