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  5. NDC Package Code: 61357-149-01 Sanafitil

NDC Package 61357-149-01 Sanafitil

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
61357-149-01
Package Description:
1 TUBE in 1 CARTON / 28.35 g in 1 TUBE
Product Code:
61357-149
Proprietary Name:
Sanafitil
Usage Information:
Clean affected area and dry thoroughly.Apply a thin layer over affected area twice daily (morning and night) or as directed by a doctor.For athlete's foot pay special attention to the space between the toes. Wear well fitting, ventilated shoes and change shoes & socks at least once a day.For athlete's foot and ringworm, use daily for 4 weeksFor jock itch use daily for 2 weeks.Supervise Children in use of this product.Product not effective in the scalp or nails.
11-Digit NDC Billing Format:
61357014901
NDC to RxNorm Crosswalk:
  • RxCUI: 1250560 - undecylenic acid 10 % Topical Ointment
  • RxCUI: 1250560 - undecylenic acid 0.1 MG/MG Topical Ointment
  • RxCUI: 1534858 - SANAFITIL Antifungal 10 % Topical Ointment
  • RxCUI: 1534858 - undecylenic acid 0.1 MG/MG Topical Ointment [Sanafitil Antifungal]
  • RxCUI: 1534858 - Sanafitil Antifungal 0.1 MG/MG Topical Ointment
    • Labeler Name:
    Zurich Medical Labs, Llc
    Sample Package:
    No
    Start Marketing Date:
    08-24-1966
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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.

    Frequently Asked Questions

    What is NDC 61357-149-01?

    The NDC Packaged Code 61357-149-01 is assigned to a package of 1 tube in 1 carton / 28.35 g in 1 tube of Sanafitil, labeled by Zurich Medical Labs, Llc. The product's dosage form is and is administered via form.

    Is NDC 61357-149 included in the NDC Directory?

    No, Sanafitil with product code 61357-149 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Zurich Medical Labs, Llc on August 24, 1966 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 61357-149-01?

    The 11-digit format is 61357014901. 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
    5-3-261357-149-015-4-261357-0149-01