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  5. NDC Package Code: 23637-001-01 Bioxsine Series

NDC Package 23637-001-01 Bioxsine Series

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:
23637-001-01
Package Description:
1 BOTTLE in 1 CARTON / 300 mL in 1 BOTTLE
Product Code:
23637-001
Proprietary Name:
Bioxsine Series
Usage Information:
Helps eliminate and reduces the recurrence of scalp itching, irritation, redness, flaking and scaling associated with dandruff.
11-Digit NDC Billing Format:
23637000101
NDC to RxNorm Crosswalk:
  • RxCUI: 426904 - zinc pyrithione 1.5 % Medicated Shampoo
  • RxCUI: 426904 - zinc pyrithione 15 MG/ML Medicated Shampoo
    • Labeler Name:
    B'iota Laboratories
    Sample Package:
    No
    Start Marketing Date:
    01-01-2012
    Listing Expiration Date:
    12-31-2018
    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 23637-001-01?

    The NDC Packaged Code 23637-001-01 is assigned to a package of 1 bottle in 1 carton / 300 ml in 1 bottle of Bioxsine Series, labeled by B'iota Laboratories. The product's dosage form is and is administered via form.

    Is NDC 23637-001 included in the NDC Directory?

    No, Bioxsine Series with product code 23637-001 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by B'iota Laboratories on January 01, 2012 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 23637-001-01?

    The 11-digit format is 23637000101. 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
    5-3-223637-001-015-4-223637-0001-01