LIDOCAINE KNEE PAIN RELIEF PATCH- lidocaine patch

Drug Labeling and Warnings

Drug Details [pdf]

Active ingredient

Lidocaine 4% ...... Purpose: Topical Anesthetic

Purpose

Topical Anesthetic

Uses

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

· more than 1 patch on your body at a time or with other topical anesthetics at the same time

· 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 this product

· use only as directed

· avoid contact with the eyes, mucous membranes, or rashes

· do not bandage tightly

· dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

Stop use if:

· localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering

· condition worsens

· symptoms persist for more than 7 days

· symptoms clear up and occur again within a few days

Ask a doctor if:

· localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering

· condition worsens

· symptoms persist for more than 7 days

· symptoms clear up and occur again within a few days

Pregnancy or breast feeding

If pregnant or breastfeeding, ask a health professional before use

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact with Poison Control Center immediately.

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 affected area.

· Carefully remove remaining film while pressing the patch firmly on the skin.

· 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 age of 12:Consult a doctor

Other information

Store at 20°C to 25°C (68°F - 77°F)

Store in a cool dry place away from direct sunlight

Inactive ingredients

Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Kaolin, Methylparaben, Polysorbate 80, PropyleneGlycol, Polyacrylic Acid, Povidone, Propylparaben, Sodium Polyacrylate, Titanium Dioxide, Tartaric Acid, Water

Questions or Comments?

supports@povihomeofficial.com

Package label. Principal display panel

INGREDIENTS AND APPEARANCE

LIDOCAINE KNEE PAIN RELIEF PATCH 
lidocaine patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87518-189
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	0.04 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
GLYCERIN (UNII: PDC6A3C0OX)
POVIDONE K90 (UNII: RDH86HJV5Z)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
EDETATE DISODIUM (UNII: 7FLD91C86K)
KAOLIN (UNII: 24H4NWX5CO)
TARTARIC ACID (UNII: W4888I119H)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87518-189-15	15 in 1 BOX	04/20/2026
1		1 in 1 BAG
1		8 g in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 87518-189-25	25 in 1 BOX	04/20/2026
2		1 in 1 BAG
2		8 g in 1 PATCH; Type 0: Not a Combination Product
3	NDC: 87518-189-35	35 in 1 BOX	04/20/2026
3		1 in 1 BOX
3		8 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/20/2026

Labeler - Guangzhou Sumi Technology Innovation Co., Ltd (518555082)

Registrant - Guangzhou Sumi Technology Innovation Co., Ltd (518555082)