United States · FDA National Drug Code directory
CICLOFERON
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
- 59208-002_24b2e848-505d-3cf9-e063-6394a90a16d7
- Product NDC
- 59208-002
- Form
- GEL
- Composition / generic term
- benzalkonium chloride and lidocaine hydrochloride
- Labeler
- Laboratorios Liomont, S.A. de C.V.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20190501
- Source listing expiry
- 20261231
Source-listed ingredients
- BENZALKONIUM CHLORIDE — 1.3 mg/g
- LIDOCAINE HYDROCHLORIDE — 20 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (59208-002-04) / 4 g in 1 TUBE · 59208-002-04
- 1 TUBE in 1 CONTAINER (59208-002-05) / 4 g in 1 TUBE · 59208-002-05
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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