feminine pain relief
Generic: menthol, unspecified form
Labeler: beyou together ltdDrug Facts
Product Profile
Brand Name
feminine pain relief
Generic Name
menthol, unspecified form
Labeler
beyou together ltd
Dosage Form
PATCH
Routes
Active Ingredients
menthol, unspecified form 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
84253-001
Product ID
84253-001_473fdd7c-e667-7f3c-e063-6294a90a5561
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2025-07-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84253001
Hyphenated Format
84253-001
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
feminine pain relief (source: ndc)
Generic Name
menthol, unspecified form (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 5 PATCH in 1 POUCH (84253-001-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "473fdd7c-e667-7f3c-e063-6294a90a5561", "openfda": {"upc": ["5060927260333"], "unii": ["L7T10EIP3A"], "rxcui": ["2621715"], "spl_set_id": ["9636b973-fe7e-481e-a6e9-8070347c0883"], "manufacturer_name": ["BeYou Together Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 PATCH in 1 POUCH (84253-001-01)", "package_ndc": "84253-001-01", "marketing_start_date": "20250714"}], "brand_name": "FEMININE PAIN RELIEF", "product_id": "84253-001_473fdd7c-e667-7f3c-e063-6294a90a5561", "dosage_form": "PATCH", "product_ndc": "84253-001", "generic_name": "MENTHOL, UNSPECIFIED FORM", "labeler_name": "BeYou Together Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FEMININE PAIN RELIEF", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "10 mg/1"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250714", "listing_expiration_date": "20261231"}