feminine pain relief
Generic: menthol, unspecified form
Labeler: unexo life sciences, private limitedDrug Facts
Product Profile
Brand Name
feminine pain relief
Generic Name
menthol, unspecified form
Labeler
unexo life sciences, private limited
Dosage Form
PATCH
Routes
Active Ingredients
menthol, unspecified form 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71391-130
Product ID
71391-130_94875a1d-da37-4c18-a673-25fa696edcf1
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2019-01-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71391130
Hyphenated Format
71391-130
Supplemental Identifiers
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
- 200 mg/1
Packaging
- 5 PATCH in 1 POUCH (71391-130-05)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "94875a1d-da37-4c18-a673-25fa696edcf1", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["30d6241f-9fca-4a1a-a509-1274007debb3"], "manufacturer_name": ["Unexo Life Sciences, Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 PATCH in 1 POUCH (71391-130-05)", "package_ndc": "71391-130-05", "marketing_start_date": "20190119"}], "brand_name": "FEMININE PAIN RELIEF", "product_id": "71391-130_94875a1d-da37-4c18-a673-25fa696edcf1", "dosage_form": "PATCH", "product_ndc": "71391-130", "generic_name": "MENTHOL, UNSPECIFIED FORM", "labeler_name": "Unexo Life Sciences, Private Limited", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FEMININE PAIN RELIEF", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "200 mg/1"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190119", "listing_expiration_date": "20261231"}