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

Open FDA National Drug Code directory

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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CICLOFERON — United States | Molindra Medicines