United States · FDA National Drug Code directory
Camphotrol
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
- 59088-488_1e2d2f1a-8848-6a76-e063-6394a90ae170
- Product NDC
- 59088-488
- Form
- GEL
- Composition / generic term
- camphor, menthol
- Labeler
- PureTek Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20220118
- Source listing expiry
- 20261231
Source-listed ingredients
- CAMPHOR (SYNTHETIC) — 4 g/100g
- MENTHOL — 10 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 85 g in 1 BOTTLE, WITH APPLICATOR (59088-488-07) · 59088-488-07
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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