69561-008

Manufacturer
Henan Kangdi Medical Devices Co., Ltd.
Effective date
2026-09-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-12 01:01:15

Label at a glance#

ProductJenGufun LIDOCAINE KNEE Patch
Active ingredientLIDOCAINE
Label structure14 sections

Dosage and administration

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

Storage and handling

■ Avoid storing product in direct sunlight ■ Protect product from excessive moisture

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

LIDOCAINE 4%

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Use

INDICATIONS & USAGE SECTION

For temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Do not use

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

When Using

OTC - WHEN USING SECTION

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

Stop Use

OTC - STOP USE SECTION

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

Ask Doctor

OTC - ASK DOCTOR SECTION

lf pregnant or breast-feeding

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Centerright away.

Directions

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

Other information

STORAGE AND HANDLING SECTION

■ Avoid storing product in direct sunlight
■ Protect product from excessive moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

Dihydroxyaluminum Aminoacetate,Edetate Disodium,Glycerin,Hydroxyacetophenone, Kaolin, L(+)-Tartaric Acid, Mineral oil.Polysorbate 80, Polyacrylic Acid,Polyvinylpyrrolidone K90,Propylene Glycol, Sodium Polyacrylate,Titanium Dioxide,Water.

Questions

OTC - QUESTIONS SECTION

Healthpatchofficial@gmail.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

69561-008

11

Products#

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

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
JenGufun LIDOCAINE KNEE PatchLIDOCAINE KNEE PATCHHenan Kangdi Medical Devices Co., Ltd.5b1d8508-b993-7a8d-e063-6294a90ae3062026-09-10WarningsExact identifier
ndc (package): 69561-008-03
ndc (package): 69561-008-01
ndc (package): 69561-008-09
ndc (package): 69561-008-02
ndc (package): 69561-008-06
ndc (package): 69561-008-10
ndc (package): 69561-008-05
ndc (package): 69561-008-07
ndc (package): 69561-008-08
ndc (package): 69561-008-04
ndc (product): 69561-008
ndc11 (package): 69561000808
ndc11 (package): 69561000803
ndc11 (package): 69561000807
ndc11 (package): 69561000805
ndc11 (package): 69561000801
ndc11 (package): 69561000809
ndc11 (package): 69561000804
ndc11 (package): 69561000802
ndc11 (package): 69561000806
ndc11 (package): 69561000810
spl id: 5b1d8508-b994-7a8d-e063-6294a90ae306
spl set id: 5b1d8508-b993-7a8d-e063-6294a90ae306

Reported adverse events (FAERS/openFDA)#

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