FDA.reportPublic FDA data

FEMININE PAIN RELIEF

Manufacturer
BeYou Together Ltd | Novamed Laboratories Private Limited
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:29:40

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 associated with: menstrual cramps lower pelvic pain backache leg cramps sprains strains

Dosage and administration

adults and children 12 years of age and older apply to the affected area no more than 2 times daily children under 12 years of age consult a doctor open pouch & remove patch peel off protective film and apply sticky side to affected area dry the skin at application area before applying the patch

Storage and handling

Avoid storing product in direct sunlight Protect product from excessive moisture

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient                                                                       Purpose

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.0%.........................................................................Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains associated with:

  • menstrual cramps
  • lower pelvic pain
  • backache
  • leg cramps
  • sprains
  • strains

Warnings

WARNINGS SECTION

For external use only
Use only as directed

Do Not Use

OTC - DO NOT USE SECTION

  • on wounds or damaged skin
  • with a heating pad

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • redness over affected area

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes, mucous membranes and rashes
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days
  • 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

  • adults and children 12 years of age and older apply to the affected area no more than 2 times daily
  • children under 12 years of age consult a doctor
  • open pouch & remove patch
  • peel off protective film and apply sticky side to affected area
  • dry the skin at application area before applying the patch

Other Information

STORAGE AND HANDLING SECTION

  • Avoid storing product in direct sunlight
  • Protect product from excessive moisture

Inactive Ingredients

INACTIVE INGREDIENT SECTION

  • adhesive Plaster
  • eucalyptus oil

Questions?

OTC - QUESTIONS SECTION

+1-303-960-2289 Mon-Thur, 10am-4pm EST

usa@beyou.co.uk


SPL UNCLASSIFIED SECTION

Distributed By:
BeYou Together Ltd,
21 Wainwright Street,
Birmingham, B6 5TH, UK

Made in India.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BEYOU Period Patches - NDC 84253-001-01 - 5 Patches Label

PRINCIPAL DISPLAY PANEL - 5 Patch Pouch LabelPRINCIPAL DISPLAY PANEL - 5 Patch Pouch Label

PRINCIPAL DISPLAY PANEL - 5 Patch Pouch LabelPRINCIPAL DISPLAY PANEL - 5 Patch Pouch Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2621715menthol 10 % Medicated PatchPSN2
2621715menthol 0.1 MG/MG Medicated PatchSCD2
2621715menthol 10 % Medicated PatchSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-135060927260333GTIN-13: 5060927260333
EAN-13: 5060927260333
GTIN storage (14 digits): 05060927260333		beyou-period-patches-label-2.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84253-001-01FEMININE PAIN RELIEF5 in 1 POUCHPATCH52

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
84253-00184253-001-01

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
EUCALYPTUS OIL2R04ONI662IACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB

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
FEMININE PAIN RELIEFMENTHOL, UNSPECIFIED FORMBeYou Together Ltd9636b973-fe7e-481e-a6e9-8070347c08832025-12-31WarningsExact identifier
ndc (package): 84253-001-01
ndc (product): 84253-001
ndc11 (package): 84253000101
spl id: 473fdd7c-e667-7f3c-e063-6294a90a5561
spl set id: 9636b973-fe7e-481e-a6e9-8070347c0883

Reported adverse events (FAERS/openFDA)#

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