Plantar Pain Relief Patch

Manufacturer
Guangzhou Sumi Technology Innovation Co., Ltd
Effective date
2026-03-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:33:59

Label at a glance#

ProductPlantar Pain Relief Patch
Active ingredientMENTHOL, LIDOCAINE
Label structure14 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

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

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

Purposes

OTC - PURPOSE SECTION

Topical anesthetic (Lidocaine)

Topical analgesic (Menthol)

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Do not use:

OTC - DO NOT USE SECTION

  • 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:

OTC - WHEN USING SECTION

  • 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:

OTC - STOP USE SECTION

  • 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,

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

· Store at 20°C to 25°C(68°F - 77°F)

· Store in a cool dry place away from direct sunlight

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

supports@povihomeofficial.com

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

patchpatch175-15175-15175-30175-30175-45175-45

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87518-17587518-175-01, 87518-175-15, 87518-175-30, 87518-175-45

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4eeb2db9-ce74-fddd-e063-6394a90a8d9d4e3a3e12-081f-7b07-e063-6294a90acdbd2026-04-07WarningsExact identifier
spl set id: 4e3a3e12-081f-7b07-e063-6294a90acdbd

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.