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  5. NDC Package Code: 43251-3351-1 Flexitol Anti Fungal

NDC Package 43251-3351-1 Flexitol Anti Fungal

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:
43251-3351-1
Package Description:
1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Code:
43251-3351
Proprietary Name:
Flexitol Anti Fungal
Usage Information:
Read all directions and warnings before useClean affected area with soap and warm water and dry thoroughlyApply a thin layer of Flexitol Anti-Fungal Liquid over the affected area twice daily (morning and night) or as directed by a doctorFor Athlete's Foot, pay special attention to the spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.For Athlete's Foot and Ringworm use daily for 4 weeks. If condition persists longer, consult a doctor.Persons under 18 years of age or those with sensitive skin should use only as directed by a doctorSupervise children in the use of this productThis product is not effective on the scalp or nailsReplace cap and tighten after each use
11-Digit NDC Billing Format:
43251335101
NDC to RxNorm Crosswalk:
  • RxCUI: 998329 - undecylenic acid 25 % Topical Solution
  • RxCUI: 998329 - undecylenic acid 250 MG/ML Topical Solution
    • Labeler Name:
    Lacorium Health International Pty Ltd
    Sample Package:
    No
    Start Marketing Date:
    01-03-2009
    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 43251-3351-1?

    The NDC Packaged Code 43251-3351-1 is assigned to a package of 1 bottle in 1 carton / 30 ml in 1 bottle of Flexitol Anti Fungal, labeled by Lacorium Health International Pty Ltd. The product's dosage form is and is administered via form.

    Is NDC 43251-3351 included in the NDC Directory?

    No, Flexitol Anti Fungal with product code 43251-3351 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Lacorium Health International Pty Ltd on January 03, 2009 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 43251-3351-1?

    The 11-digit format is 43251335101. 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 5-4-1 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
    5-4-143251-3351-15-4-243251-3351-01