NDC Package 59469-138-30 Zellulisan

Arnica Montana Root,Ledum Palustre Twig,Toxicodendron Pubescens Shoot,Sulfur,Horse - View Billable Units, 11-Digit Format, RxNorm

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:
59469-138-30
Package Description:
1 TUBE in 1 BOX / 30 g in 1 TUBE
Product Code:
Proprietary Name:
Zellulisan
Non-Proprietary Name:
Arnica Montana Root, Ledum Palustre Twig, Toxicodendron Pubescens Shoot, Sulfur, Horse Chestnut, Betula Pendula Leaf, Hedera Helix Flowering Twig, And Melilotus Officinalis Top
Substance Name:
Arnica Montana Root; Betula Pendula Leaf; Hedera Helix Flowering Twig; Horse Chestnut; Melilotus Officinalis Top; Rhododendron Tomentosum Leafy Twig; Sulfur; Toxicodendron Pubescens Shoot
Usage Information:
Unless otherwise prescribed, apply a moderate amount of ointment 2 to 3 times per day by rubbing gently into the affected area.
11-Digit NDC Billing Format:
59469013830
Product Type:
Human Otc Drug
Labeler Name:
Pekana Naturheilmittel Gmbh
Dosage Form:
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
  • Cutaneous - Administration to the skin.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    12-11-2008
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    59469-138-401 TUBE in 1 BOX / 100 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 59469-138-30?

    The NDC Packaged Code 59469-138-30 is assigned to a package of 1 tube in 1 box / 30 g in 1 tube of Zellulisan, a human over the counter drug labeled by Pekana Naturheilmittel Gmbh. The product's dosage form is ointment and is administered via cutaneous form.

    Is NDC 59469-138 included in the NDC Directory?

    Yes, Zellulisan with product code 59469-138 is active and included in the NDC Directory. The product was first marketed by Pekana Naturheilmittel Gmbh on December 11, 2008 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 59469-138-30?

    The 11-digit format is 59469013830. 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
    5-3-259469-138-305-4-259469-0138-30