United States · FDA National Drug Code directory
Lubracane
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
- 72235-5838_a0727e5c-e1ae-4e4c-a757-25e3c5f83a89
- Product NDC
- 72235-5838
- Form
- GEL
- Composition / generic term
- Lubracane
- Labeler
- Ozeion LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20180115
- Source listing expiry
- 20271231
Source-listed ingredients
- MENTHOL — .24 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 118.3 mL in 1 JAR (72235-5838-1) · 72235-5838-1
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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