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RWSEFK Lidocaine Pain Relief Gel-Patch

Dosage form
PATCH
Labeler
Henan Enokon Medical Instrument Co., Ltd.
Label updated
2025-03-25
Retrieved
2026-09-07
Active ingredients
LIDOCAINE
View original label and images on DailyMed ↗
Active Ingredient

Lidocaine 4%

Purpose

Topical anesthetic

Use

Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.

Warnings

For external use only

Do not use

Do not use
on wounds or damaged skin
with a heating pad or device
with other ointments, creams, sprays, or liniments
if you are allergic to any ingredients of this product

When Using

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

Stop Use

Stop use and ask a doctor if
on wounds or damaged skin
with a heating pad or device
with other ointments, creams, sprays, or liniments
if you are allergic to any ingredients of this product

Ask Doctor

If pregnant or breast-feeding, ask a health professional before use.
Children under age of 12: Consult a doctor

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.
If swallowed accidentally, get medical help or contact with Poison Control Center immediately.

Directions

Directions
Adults and Children above 12 years old:
Clean and dry the affected area.
Tear off the protective film and apply the exposed part of the patch to the the affected area.
Carefully remove remaining film while pressing the patch firmly on the skin.
Remove patch from the skin after at most 8-hour application.

Inactive ingredients

Inactive Ingredients
Glycerin,Sodium polyacrylate,Polyvinyl pyrrolidone,Phenoxyethanol,Tartaric Acid,Ethyl ethyl glycerol,Sodium carboxymethyl cellulose,Aluminum Glycinate,Styrene acrylic copolymer emulsion,EDTA,Titanium Dioxide,Polysorbate 80,Sorbitol,Purified Water

PRINCIPAL DISPLAY PANEL

[Image in the official label — see DailyMed source]

PRINCIPAL DISPLAY PANEL

[Image in the official label — see DailyMed source]

DailyMed Set ID: 31366793-f8a6-a2c4-e063-6294a90acbfc · Version 1
NDC: 83559-008