Sumi-Plantar Pain Relief Patch

Plantar Pain Relief Patch by

Drug Labeling and Warnings

Plantar Pain Relief Patch by is a Otc medication manufactured, distributed, or labeled by Guangzhou Sumi Technology Innovation Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PLANTAR PAIN RELIEF PATCH- lidocaine and menthol patch 
Guangzhou Sumi Technology Innovation Co., Ltd

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Sumi-Plantar Pain Relief Patch

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

patch175-15175-30175-45

PLANTAR PAIN RELIEF PATCH 
lidocaine and menthol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 87518-175
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.01 g  in 1 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE0.04 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
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
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 87518-175-1515 in 1 BOX03/30/2026
11 in 1 BAG
1NDC: 87518-175-0121 g in 1 PATCH; Type 0: Not a Combination Product
2NDC: 87518-175-3030 in 1 BOX03/30/2026
21 in 1 BAG
2NDC: 87518-175-0121 g in 1 PATCH; Type 0: Not a Combination Product
3NDC: 87518-175-4545 in 1 BOX03/30/2026
31 in 1 BAG
3NDC: 87518-175-0121 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/30/202603/30/2026
Labeler - Guangzhou Sumi Technology Innovation Co., Ltd (518555082)
Registrant - Guangzhou Sumi Technology Innovation Co., Ltd (518555082)

Revised: 4/2026
 
Guang

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