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JenGufun LIDOCAINE KNEE Patch drug information

LIDOCAINE KNEE PATCH
Henan Kangdi Medical Devices Co., Ltd. · TOPICAL

Product NDC: 69561-008

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameLIDOCAINE KNEE PATCH
Labeler / manufacturerHenan Kangdi Medical Devices Co., Ltd.
RouteTOPICAL
Drug classAmide Local Anesthetic / Antiarrhythmic
Product NDC69561-008
Label effective date2026-09-10

Official product label reference

JenGufun LIDOCAINE KNEE Patch — Henan Kangdi Medical Devices Co., Ltd.

This page contains 13 source sections for LIDOCAINE KNEE PATCH, topical route. Label set 5b1d8508-b993-7a8d-e063-6294a90ae306, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use For temporary relief of pain

Purpose

Purpose Topical anesthetic
Dosage and administration — label text
Directions 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
Warnings
Warnings For external use only
Active ingredient
Active Ingredient LIDOCAINE 4%
Do not use
Do not use ■ 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
While using this medicine
When Using ■ use only as directed ■ avoid contact with the eyes, mucous membranes, or rashes ■ do not bandage tightly
When to stop use and seek help
Stop Use ■ 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 a doctor before use
Ask Doctor lf pregnant or breast-feeding
Child safety
Keep Out Of Reach Of Children If swallowed, get medical help or contact a Poison Control Centerright away.
Storage and handling
Other information ■ Avoid storing product in direct sunlight ■ Protect product from excessive moisture
Inactive ingredient
Inactive ingredients 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
Questions Healthpatchofficial@gmail.com

Official sources and product identifiers

Substances listed: LIDOCAINE

RxNorm identifiers: 1737778

Package NDC codes

69561-008-01, 69561-008-02, 69561-008-03, 69561-008-04, 69561-008-05, 69561-008-06, 69561-008-07, 69561-008-08, 69561-008-09, 69561-008-10

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.