MENTHOL PAIN RELIEF Gel-Patch

Manufacturer
Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
Effective date
2021-08-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:37:21

Label at a glance#

ProductMENTHOL PAIN RELIEF Gel-Patch
Active ingredientMENTHOL
Label structure16 sections

Indications and uses

Temporary relief from minor aches and pains of sore muscles and joints associated with: arthrits backache strains sprains

Dosage and administration

Adult and Children 12 years of age and older : Clean and dry affected area, partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing patch to skin and leave in place for up to 8 hours. Use on affected areas not more than 4 times daily. Wash hands with cool water after use. Children under 12 years of age : Consult physician

Storage and handling

Store in a cool dry place away from direct sunlight

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 5.6% ...... Purpose: Topical Analgesic

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporary relief from minor aches and pains of sore muscles and joints associated with:

  • arthrits
  • backache
  • strains
  • sprains

Warnings

WARNINGS SECTION

  • For external use only
  • Use only as directed
  • Do not bandage tightly or use with heating pad or device
  • Avoid contact with eyes or mucous membranes
  • Do not apply to wounds or damaged skin
  • Do not use with other ointments, creams, sprays, or liniments
  • Do not apply to irritated skin

Ask doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have: Sensitive skin

Stop use and ask a doctor if: Burning disconfort or excessive skin irritation develops, condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days

If pregnant or breast-feeding: Ask a health professional before use

When using

OTC - WHEN USING SECTION

For external use only

  • Use only as directed
  • Do not bandage tightly or use with heating pad or device
  • Avoid contact with eyes or mucous membranes
  • Do not apply to wounds or damaged skin
  • Do not use with other ointments, creams, sprays, or liniments
  • Do not apply to irritated skin

Do not use

OTC - DO NOT USE SECTION

  • Use only as directed
  • Do not bandage tightly or use with heating pad or device
  • Avoid contact with eyes or mucous membranes
  • Do not apply to wounds or damaged skin
  • Do not use with other ointments, creams, sprays, or liniments
  • Do not apply to irritated skin

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if: Burning disconfort or excessive skin irritation develops, condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days

Pregnancy or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding: Ask a health professional before use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: If accidentally ingested, get medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adult and Children 12 years of age and older: Clean and dry affected area, partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing patch to skin and leave in place for up to 8 hours. Use on affected areas not more than 4 times daily. Wash hands with cool water after use.
  • Children under 12 years of age: Consult physician

Dosage forms & strengths

DOSAGE FORMS & STRENGTHS SECTION

This is patch dosage form.

The active ingredient strength is 5%.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Polyacrylic acid, Propylene glycol, Sodium polyacrylate, Mineral oil, Polysorbate 80, PVP, Petrolatum, Dihydroxyaluminum aminoacetate, Edetate disodium, Kaolin, Carboxymethylcellulose sodium, Titanium dioxide,
L-Tartaric acid, Benzalkonium chloride, Lauralkonium chloride, Aloe barbadensis leaf extract, Arnica montana flower extract, Boswellia carterii resin extract, Camellia sinensis leaf extract

Questions

OTC - QUESTIONS SECTION

Questions or comments: 86-21-31166566

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool dry place away from direct sunlight

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage LabelContainer LabelContainer Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73557-13873557-138-01, 73557-138-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
f105652c-7363-660c-e053-2995a90a1c4ec9eab65a-708a-a149-e053-2995a90a8ade2022-12-29WarningsExact identifier
spl set id: c9eab65a-708a-a149-e053-2995a90a8ade

Reported adverse events (FAERS/openFDA)#

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