FDA.reportPublic FDA data

FEMININE PAIN RELIEF PATCH - 50 cm2

Manufacturer
Unexo Life Sciences Private Limited
Effective date
2024-03-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:09:39

Label at a glance#

ProductFEMININE PAIN RELIEF
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure10 sections

Indications and uses

For temporary relief of minor aches and pains in lower back and abdomen associated with cramps.

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 off 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

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Uses

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains in lower back and abdomen associated with cramps.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

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 off 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

Other Information

STORAGE AND HANDLING SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Adhesive Plaster, Eucalyptus Oil

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 4 Patch Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 71391-131-04

UNEXO LIFE SCIENCES

FEMININE PAIN RELIEF PATCH
50 cm2

MENTHOL

SOOTHE PERIOD CRAMPS
FAST ACTING
APPLY FOR 8-12 HOURS

4 PATCHES

PRINCIPAL DISPLAY PANEL - 4 Patch Pouch Label
PRINCIPAL DISPLAY PANEL - 4 Patch Pouch Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2621715menthol 10 % Medicated PatchPSN1
2621715menthol 0.1 MG/MG Medicated PatchSCD1
2621715menthol 10 % Medicated PatchSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71391-131-04FEMININE PAIN RELIEF4 in 1 POUCHPATCH41
71391-131-24FEMININE PAIN RELIEF24 in 1 BOXPATCH241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71391-131FEMININE PAIN RELIEF (MENTHOL, UNSPECIFIED FORM) PATCH [UNEXO LIFE SCIENCES PRIVATE LIMITED]12 package rows20240312_2dccf5b6-98e1-4bf0-9c70-e3b37c468446.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71391-13171391-131-04, 71391-131-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
Eucalyptus oil2R04ONI662IACT

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
4adb8ea5-da26-45b5-bffb-6d15360907862dccf5b6-98e1-4bf0-9c70-e3b37c4684462026-07-27WarningsExact identifier
spl set id: 2dccf5b6-98e1-4bf0-9c70-e3b37c468446

Reported adverse events (FAERS/openFDA)#

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