PLANTAR PAIN RELIEF PATCH- lidocaine and menthol patch

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Lidocaine 4% ...... Purpose: Topical anesthetic

Menthol 1% ...... Purpose: Topical analgesic

Purposes

Topical anesthetic (Lidocaine)

Topical analgesic (Menthol)

Uses

For the temporary relief of minor aches and pains (associated with plantar fasciitis, arch pain, heel pain).

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 and ask a doctor if:

• 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

If pregnant or breast-feeding,

Ask a health professional before use

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adult and Children above12 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 morethan 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

Dihydroxyaluminium Aminoacetate, Edetate Disodium, Glycerin, Hydroxyacetophenone,Kaolin, L(+)-Tartaric Acid, Mineral oil, Polysorbate80, Polyacrylic Acid , Polyvinylpyrrolidone K90,Propylene Glycol, Sodium Polyacrylate,Titanium Dioxide, Water.

Questions or Comments

supports@povihomeofficial.com

Package label. Principal display panel

INGREDIENTS AND APPEARANCE

PLANTAR PAIN RELIEF PATCH 
lidocaine and menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87518-174
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.01 g  in 1 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	0.04 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TARTARIC ACID (UNII: W4888I119H)
WATER (UNII: 059QF0KO0R)
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
MINERAL OIL (UNII: T5L8T28FGP)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
KAOLIN (UNII: 24H4NWX5CO)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POVIDONE K90 (UNII: RDH86HJV5Z)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87518-174-15	15 in 1 BOX	03/30/2026
1		1 in 1 BAG
1	NDC: 87518-174-01	6 g in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 87518-174-30	30 in 1 BOX	03/30/2026
2		1 in 1 BAG
2	NDC: 87518-174-01	6 g in 1 PATCH; Type 0: Not a Combination Product
3	NDC: 87518-174-45	45 in 1 BOX	03/30/2026
3		1 in 1 BAG
3	NDC: 87518-174-01	6 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	03/30/2026

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

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