cicloferon

Generic: benzalkonium chloride and lidocaine hydrochloride

Labeler: laboratorios liomont, s.a. de c.v.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cicloferon
Generic Name benzalkonium chloride and lidocaine hydrochloride
Labeler laboratorios liomont, s.a. de c.v.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

benzalkonium chloride 1.3 mg/g, lidocaine hydrochloride 20 mg/g

Manufacturer
Laboratorios Liomont, S.A. de C.V.

Identifiers & Regulatory

Product NDC 59208-002
Product ID 59208-002_24b2e848-505d-3cf9-e063-6394a90a16d7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M003
Listing Expiration 2026-12-31
Marketing Start 2019-05-01

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59208002
Hyphenated Format 59208-002

Supplemental Identifiers

RxCUI
1431682 1431687
UNII
F5UM2KM3W7 V13007Z41A

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cicloferon (source: ndc)
Generic Name benzalkonium chloride and lidocaine hydrochloride (source: ndc)
Application Number M003 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.3 mg/g
  • 20 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (59208-002-04) / 4 g in 1 TUBE
  • 1 TUBE in 1 CONTAINER (59208-002-05) / 4 g in 1 TUBE
source: ndc

Packages (2)

59208-002-04 1 TUBE in 1 CARTON (59208-002-04) / 4 g in 1 TUBE 59208-002-05 1 TUBE in 1 CONTAINER (59208-002-05) / 4 g in 1 TUBE

Ingredients (2)

benzalkonium chloride (1.3 mg/g) lidocaine hydrochloride (20 mg/g)

Linked Drug Pages (1)

CICLOFERON ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "24b2e848-505d-3cf9-e063-6394a90a16d7", "openfda": {"unii": ["F5UM2KM3W7", "V13007Z41A"], "rxcui": ["1431682", "1431687"], "spl_set_id": ["89081ef8-9721-a476-e053-2995a90ae0de"], "manufacturer_name": ["Laboratorios Liomont, S.A. de C.V."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59208-002-04)  / 4 g in 1 TUBE", "package_ndc": "59208-002-04", "marketing_start_date": "20190501"}, {"sample": false, "description": "1 TUBE in 1 CONTAINER (59208-002-05)  / 4 g in 1 TUBE", "package_ndc": "59208-002-05", "marketing_start_date": "20190501"}], "brand_name": "CICLOFERON", "product_id": "59208-002_24b2e848-505d-3cf9-e063-6394a90a16d7", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59208-002", "generic_name": "benzalkonium chloride and lidocaine hydrochloride", "labeler_name": "Laboratorios Liomont, S.A. de C.V.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CICLOFERON", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/g"}, {"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/g"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}