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  5. NDC Package Code: 59208-002-04 Cicloferon

NDC Package 59208-002-04 Cicloferon

Benzalkonium Chloride And Lidocaine Hydrochloride Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
59208-002-04
Package Description:
1 TUBE in 1 CARTON / 4 g in 1 TUBE
Product Code:
59208-002
Proprietary Name:
Cicloferon
Non-Proprietary Name:
Benzalkonium Chloride And Lidocaine Hydrochloride
Substance Name:
Benzalkonium Chloride; Lidocaine Hydrochloride
Usage Information:
Clean the affected areaapply a small amount of this product to the affected area 1 to 3 times dailymay be covered with a sterile bandagechildren under 12 years of age, consult a doctor
11-Digit NDC Billing Format:
59208000204
NDC to RxNorm Crosswalk:
  • RxCUI: 1431682 - benzalkonium chloride 0.13 % / lidocaine HCl 2 % Topical Gel
  • RxCUI: 1431682 - benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.02 MG/MG Topical Gel
  • RxCUI: 1431682 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 2 % Topical Gel
  • RxCUI: 1431687 - CICLOFERON 0.13 % / 2 % Topical Gel
  • RxCUI: 1431687 - benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.02 MG/MG Topical Gel [Cicloferon]
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Laboratorios Liomont, S.a. De C.v.
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • BENZALKONIUM CHLORIDE 1.3 mg/g
  • LIDOCAINE HYDROCHLORIDE 20 mg/g
    • Pharmacologic Class(es):
  • Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
  • Amides - [CS]
  • Antiarrhythmic - [EPC] (Established Pharmacologic Class)
  • Local Anesthesia - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    05-01-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    59208-002-051 TUBE in 1 CONTAINER / 4 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 59208-002-04?

    The NDC Packaged Code 59208-002-04 is assigned to a package of 1 tube in 1 carton / 4 g in 1 tube of Cicloferon, a human over the counter drug labeled by Laboratorios Liomont, S.a. De C.v.. The product's dosage form is gel and is administered via topical form.

    Is NDC 59208-002 included in the NDC Directory?

    Yes, Cicloferon with product code 59208-002 is active and included in the NDC Directory. The product was first marketed by Laboratorios Liomont, S.a. De C.v. on May 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 59208-002-04?

    The 11-digit format is 59208000204. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-259208-002-045-4-259208-0002-04