menthol

Generic: menthol

Labeler: sunset pain relief roll-on 3oz
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name menthol
Generic Name menthol
Labeler sunset pain relief roll-on 3oz
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

menthol, unspecified form 4 g/100mL

Manufacturer
SUNSET PAIN RELIEF ROLL-ON 3OZ

Identifiers & Regulatory

Product NDC 72937-004
Product ID 72937-004_44141d2a-1d91-b970-e063-6294a90a53f4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Marketing Start 2019-09-24
Marketing End 2026-10-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72937004
Hyphenated Format 72937-004

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 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 (72937-004-03)
source: ndc

Packages (1)

72937-004-03 90 mL in 1 BOTTLE, WITH APPLICATOR (72937-004-03)

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": "44141d2a-1d91-b970-e063-6294a90a53f4", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["934d4638-b47b-187d-e053-2995a90ae69d"], "manufacturer_name": ["SUNSET PAIN RELIEF ROLL-ON 3OZ"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 mL in 1 BOTTLE, WITH APPLICATOR (72937-004-03)", "package_ndc": "72937-004-03", "marketing_end_date": "20261023", "marketing_start_date": "20190924"}], "brand_name": "MENTHOL", "product_id": "72937-004_44141d2a-1d91-b970-e063-6294a90a53f4", "dosage_form": "GEL", "product_ndc": "72937-004", "generic_name": "MENTHOL", "labeler_name": "SUNSET PAIN RELIEF ROLL-ON 3OZ", "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_end_date": "20261023", "marketing_start_date": "20190924"}