Menthol 10% FEMININE PAIN RELIEF PATCH Drug Facts

Manufacturer
Novamed Laboratories Private Limited
Effective date
2025-08-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:54

Label at a glance#

ProductFEMININE PAIN RELIEF
Active ingredientMENTHOL
Label structure14 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 dry the skin at application area before applying the patch open pouch and remove patch peel off protective film and apply sticky side to affected area children under 12 years of age consult a doctor

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient (in each patch)                  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 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 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, get medical help or contact a Poison Control Center (1-800-222-1222) 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
  • dry the skin at application area before applying the patch
  • open pouch and remove patch
  • peel off protective film and apply sticky side to affected area
  • children under 12 years of age consult a doctor

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

OTC - QUESTIONS SECTION

Questions or CommentsCall +91 1276 457643

SPL UNCLASSIFIED SECTION

Manufactured By:
Novamed Laboratories Pvt. Ltd.
Plot No. 03, Sector 16, HSIIDC Industrial Estate,
Bahadurgarh, Haryana – 124507 (India)

MADE IN INDIA

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Menthol 10% Topical Analgesic Feminine Pain Relief Patch- NDC 85267-005-01 - Pouch Label

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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
85267-00585267-005-01, 85267-005-05, 85267-005-10

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
MENTHOLL7T10EIP3AACTIB

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
3ccc05b3-6210-d6f1-e063-6394a90a54f50c08bc4f-b99f-40cf-9cd7-06e2e8ad808f2025-08-20WarningsExact identifier
spl id: 3ccc05b3-6210-d6f1-e063-6394a90a54f5
spl set id: 0c08bc4f-b99f-40cf-9cd7-06e2e8ad808f

Reported adverse events (FAERS/openFDA)#

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