FDA.reportPublic FDA data

PAIN RELIEF

Manufacturer
Unexo Life Sciences, Private Limited
Effective date
2021-01-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:36:59

Label at a glance#

ProductPAIN RELIEF
Active ingredientMENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (SYNTHETIC)
Label structure9 sections

Indications and uses

For temporary relief of minor aches and pains of muscles and joints associated with: Simple backache | Arthritis | Sprains | Strains | Bruises

Dosage and administration

For use by Adults and Children 12 years of age and older Apply to the affected area no more than 2 times a day Dry skin completely at application area, before applying the patch Open pouch and remove patch Peel of protective film and apply sticky side to affected area If applied on hairy skin, remove gently using mild warm water Patch once used, cannot be re-pasted or reused Dispose properly after use Children und...

Storage and handling

Store at room temperature below 80°F (27°C)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active IngredientPurpose
Menthol 7%Topical Analgesic
Wintergreen Oil 7%Topical Analgesic
Camphor 7%Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints associated with: Simple backache | Arthritis | Sprains | Strains | Bruises

Warnings

WARNINGS SECTION

For External Use Only.

Do not use otherwise than as directed.

Do Not Use

OTC - DO NOT USE SECTION

  • On open wounds, cuts, eyes and face
  • With a heating pad

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes and mucous membranes
  • Do not bandage tightly

Ask Your Doctor Before Use if you have

OTC - ASK DOCTOR SECTION

  • redness over the affected area
  • have sensitive skin
  • are pregnant or breast-feeding

Stop Use and Ask Your Doctor

OTC - STOP USE SECTION

  • If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days
  • If abnormal skin irritation occurs after usage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children.

If swallowed, seek medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • For use by Adults and Children 12 years of age and older
  • Apply to the affected area no more than 2 times a day
  • Dry skin completely at application area, before applying the patch
  • Open pouch and remove patch
  • Peel of protective film and apply sticky side to affected area
  • If applied on hairy skin, remove gently using mild warm water
  • Patch once used, cannot be re-pasted or reused
  • Dispose properly after use
  • Children under 12 years of age, consult a doctor

Other Information

STORAGE AND HANDLING SECTION

  • Store at room temperature below 80°F (27°C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Adhesive Plaster

SPL UNCLASSIFIED SECTION

Manufactured By:
Unexo Life Sciences Pvt. Ltd.
B-16, Sector 4, Bawana Industrial Area,
Delhi -110039 (INDIA)

PRINCIPAL DISPLAY PANEL - 3 Patch Pouch

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 71391-135-03

unexo®
LIFE SCIENCES

PAIN RELIEF PATCH
MEDICATED | FAST ACTING

Lower Back
Joints
Upper Back
Shoulder
Elbow

APPLY FOR 8-12 HOURS

3 PATCHES
LARGE

PLEASE RESEAL AFTER OPENING

PRINCIPAL DISPLAY PANEL - 3 Patch Pouch
PRINCIPAL DISPLAY PANEL - 3 Patch Pouch

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71391-135-032023-01-30C16284748780-1f386c649-d8f0-0266-e053-dadaa90a7c1aPAIN RELIEF

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71391-135-03PAIN RELIEF3 in 1 POUCHPATCH32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71391-135PAIN RELIEF (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND CAMPHOR (SYNTHETIC)) PATCH [UNEXO LIFE SCIENCES, PRIVATE LIMITED]2Legacy NDC, 1 package rows20210116_b409dcf0-9309-490e-8ac2-9de81f006318.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71391-13571391-135-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB

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
49a22fe4-66ac-4f36-8403-cfaef0a2423eb409dcf0-9309-490e-8ac2-9de81f0063182026-07-27WarningsExact identifier
spl set id: b409dcf0-9309-490e-8ac2-9de81f006318

Reported adverse events (FAERS/openFDA)#

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