United States · FDA National Drug Code directory
MENTHOL
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72937-004_44141d2a-1d91-b970-e063-6294a90a53f4
- Product NDC
- 72937-004
- Form
- GEL
- Composition / generic term
- MENTHOL
- Labeler
- SUNSET PAIN RELIEF ROLL-ON 3OZ
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20190924 / 20261023
Source-listed ingredients
- MENTHOL, UNSPECIFIED FORM — 4 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 90 mL in 1 BOTTLE, WITH APPLICATOR (72937-004-03) · 72937-004-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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