FEMININE PAIN RELIEF- menthol, unspecified form patch

FEMININE PAIN RELIEF by

Drug Labeling and Warnings

FEMININE PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by BeYou Together Ltd, Novamed Laboratories Private Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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DRUG FACTS

Active Ingredient                                                                       Purpose

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

Uses

For temporary relief of minor aches and pains associated with:

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

PURPOSE

Warnings

For external use only
Use only as directed

Do Not Use

• on wounds or damaged skin
• with a heating pad

Ask a doctor before use if you have

• redness over affected area

When using this product

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

Stop use and ask a doctor if

• 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

Keep out of reach of children.If swallowed, seek medical help or contact a Poison Control Center right away.

Directions

• 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

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

Inactive Ingredients

• adhesive Plaster
• eucalyptus oil

Questions?

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

usa@beyou.co.uk

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

Made in India.

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

FEMININE PAIN RELIEF 
menthol, unspecified form patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84253-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	10 mg

Inactive Ingredients
Ingredient Name	Strength
EUCALYPTUS OIL (UNII: 2R04ONI662)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84253-001-01	5 in 1 POUCH; Type 0: Not a Combination Product	07/14/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/14/2025

Labeler - BeYou Together Ltd (223353507)

Establishment
Name	Address	ID/FEI	Business Operations
Novamed Laboratories Private Limited		766401623	manufacture(84253-001) , analysis(84253-001) , label(84253-001) , pack(84253-001)