feminine pain relief

Generic: menthol, unspecified form

Labeler: unexo life sciences, private limited
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name feminine pain relief
Generic Name menthol, unspecified form
Labeler unexo life sciences, private limited
Dosage Form PATCH
Routes
TOPICAL
Active Ingredients

menthol, unspecified form 200 mg/1

Manufacturer
Unexo Life Sciences, Private Limited

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
L7T10EIP3A

Packaging Origin

Original Packager
true

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
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 5 PATCH in 1 POUCH (71391-130-05)
source: ndc

Packages (1)

Ingredients (1)

menthol, unspecified form (200 mg/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"}