Flexitol Anti Fungal
NDC Package 43251-3351-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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.

Flexitol Anti Fungal is 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. Marketed by Lacorium Health International Pty Ltd, this product is identified by NDC 43251-3351 and is authorized under FDA application part333C.

Identification & Billing

NDC Package Code
43251-3351-1
Package Description
1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Code
43251-3351
11-Digit Billing Format
43251335101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Flexitol Anti Fungal
Dosage Form
-
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

Regulatory & Marketing

Labeler Name
Lacorium Health International Pty Ltd
FDA Application #
part333C
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-03-2009
Listing Expiration
12-31-2017
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43251-3351-1 identifies a specific commercial package of 1 bottle in 1 carton / 30 ml in 1 bottle of Flexitol Anti Fungal, labeled by Lacorium Health International Pty Ltd. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Lacorium Health International Pty Ltd on January 03, 2009. The current certification is valid through December 31, 2017.

How is this Lacorium Health International Pty Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43251335101. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
43251-3351-1
11-Digit CMS (5-4-2)
43251-3351-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.