menthol

Generic: menthol

Labeler: sunset pain relief
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name menthol
Generic Name menthol
Labeler sunset pain relief
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

menthol, unspecified form 4 g/100mL

Manufacturer
SUNSET PAIN RELIEF

Identifiers & Regulatory

Product NDC 72937-632
Product ID 72937-632_45c5ca7e-20df-92db-e063-6294a90ac402
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2025-12-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72937632
Hyphenated Format 72937-632

Supplemental Identifiers

UPC
0875292791727
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 menthol (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 4 g/100mL
source: ndc
Packaging
  • 90 mL in 1 BOTTLE, WITH APPLICATOR (72937-632-03)
source: ndc

Packages (1)

72937-632-03 90 mL in 1 BOTTLE, WITH APPLICATOR (72937-632-03)

Ingredients (1)

menthol, unspecified form (4 g/100mL)

Linked Drug Pages (1)

MENTHOL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "45c5ca7e-20df-92db-e063-6294a90ac402", "openfda": {"upc": ["0875292791727"], "unii": ["L7T10EIP3A"], "spl_set_id": ["45c5ca6f-d425-6cfb-e063-6394a90a1b66"], "manufacturer_name": ["SUNSET PAIN RELIEF"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 mL in 1 BOTTLE, WITH APPLICATOR (72937-632-03)", "package_ndc": "72937-632-03", "marketing_start_date": "20251220"}], "brand_name": "MENTHOL", "product_id": "72937-632_45c5ca7e-20df-92db-e063-6294a90ac402", "dosage_form": "GEL", "product_ndc": "72937-632", "generic_name": "MENTHOL", "labeler_name": "SUNSET PAIN RELIEF", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MENTHOL", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "4 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251220", "listing_expiration_date": "20261231"}