United States · FDA National Drug Code directory
ORCA Complete Menthol Pain Reliever
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
- 82939-000_0c06e3d2-4481-f4b5-e063-6394a90a0608
- Product NDC
- 82939-000
- Form
- LIQUID
- Composition / generic term
- MENTHOL
- Labeler
- ORCA Products, LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20220915
- Source listing expiry
- 20261231
Source-listed ingredients
- MENTHOL, UNSPECIFIED FORM — 20 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 BOX (82939-000-02) / 13 mL in 1 BOTTLE · 82939-000-02
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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