FEMININE PAIN RELIEF

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: FEMININE PAIN RELIEF
Generic name: MENTHOL, UNSPECIFIED FORM
Manufacturer: BeYou Together Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 9636b973-fe7e-481e-a6e9-8070347c0883
SPL ID: 473fdd7c-e667-7f3c-e063-6294a90a5561
Version: 2
Effective date: 2025-12-31
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:46:47

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		FEMININE PAIN RELIEF	openfda.brand_name
generic name		MENTHOL, UNSPECIFIED FORM	openfda.generic_name
manufacturer name		BeYou Together Ltd	openfda.manufacturer_name
ndc	package	84253-001-01	openfda.package_ndc
ndc	product	84253-001	openfda.product_ndc
ndc11	package	84253000101	derived:openfda.package_ndc
rxcui		2621715	openfda.rxcui
spl id		473fdd7c-e667-7f3c-e063-6294a90a5561	id
spl set id		9636b973-fe7e-481e-a6e9-8070347c0883	set_id
unii		L7T10EIP3A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

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