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  5. NDC Package Code: 71399-6586-3 Onelax Fiber Therapy Original Coarse

NDC Package 71399-6586-3 Onelax Fiber Therapy Original Coarse

Psyllium Husk Powder Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
71399-6586-3
Package Description:
368 g in 1 BOTTLE, PLASTIC
Product Code:
71399-6586
Proprietary Name:
Onelax Fiber Therapy Original Coarse
Non-Proprietary Name:
Psyllium Husk
Substance Name:
Psyllium Husk
Usage Information:
This medication is used to treat constipation. It increases the bulk in your stool, an effect that helps to cause movement of the intestines. It also works by increasing the amount of water in the stool, making the stool softer and easier to pass. Psyllium, one type of bulk-forming laxative, has also been used along with a proper diet to treat high cholesterol.
11-Digit NDC Billing Format:
71399658603
NDC to RxNorm Crosswalk:
  • RxCUI: 824586 - psyllium 3.4 GM Powder for Oral Suspension
  • RxCUI: 824586 - psyllium 3400 MG Powder for Oral Suspension
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Akron Pharma Inc.
    Dosage Form:
    Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • PSYLLIUM HUSK 3.4 g/7g
    • Sample Package:
    No
    FDA Application Number:
    part334
    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:
    01-01-2023
    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.

    Frequently Asked Questions

    What is NDC 71399-6586-3?

    The NDC Packaged Code 71399-6586-3 is assigned to a package of 368 g in 1 bottle, plastic of Onelax Fiber Therapy Original Coarse, a human over the counter drug labeled by Akron Pharma Inc.. The product's dosage form is powder and is administered via oral form.

    Is NDC 71399-6586 included in the NDC Directory?

    Yes, Onelax Fiber Therapy Original Coarse with product code 71399-6586 is active and included in the NDC Directory. The product was first marketed by Akron Pharma Inc. on January 01, 2023 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 71399-6586-3?

    The 11-digit format is 71399658603. 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
    5-4-171399-6586-35-4-271399-6586-03