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  5. NDC Package Code: 50114-7030-2 Zeel

NDC Package 50114-7030-2 Zeel

Arnica Montana Root,Toxicodendron Pubescens Leaf,Solanum Dulcamara Top,Comfrey - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
50114-7030-2
Package Description:
3 AMPULE in 1 CARTON / 2 mL in 1 AMPULE
Product Code:
50114-7030
Proprietary Name:
Zeel
Non-Proprietary Name:
Arnica Montana Root, Toxicodendron Pubescens Leaf, Solanum Dulcamara Top, Comfrey Root, Sulfur, Sanguinaria Canadensis Root, Sus Scrofa Cartilage, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Sus Scrofa Placenta, .alpha.-lipoic Acid, Coenzyme A, Nadide And Sodium Diethyl Oxalacetate
Substance Name:
.alpha.-lipoic Acid; Arnica Montana Root; Coenzyme A; Comfrey Root; Nadide; Sanguinaria Canadensis Root; Sodium Diethyl Oxalacetate; Solanum Dulcamara Top; Sulfur; Sus Scrofa Cartilage; Sus Scrofa Embryo; Sus Scrofa Placenta; Sus Scrofa Umbilical Cord; Toxicodendron Pubescens Leaf
Usage Information:
Treatment of arthrosis/osteoarthritis, and/or rheumatic joint diseasesZeel® Injection Solution is a homeopathic drug product indicated for the treatment of arthrosis/osteoarthritis, and/or rheumatic joint diseases and for the relief of symptoms such as pain and joint stiffness.Co-administration Therapy with Traumeel® Injection Solution for the treatment of inflammatory and degenerative conditions of the musculoskeletal system.Zeel® Injection Solution is a homeopathic drug product indicated, in combination with Traumeel® Injection Solution, for the treatment of inflammatory and degenerative conditions of the musculoskeletal system, such as arthrosis/osteoarthritis and/or rheumatic joint diseases, and for the relief of symptoms including pain, swelling, and joint stiffness.
11-Digit NDC Billing Format:
50114703002
Product Type:
Human Prescription Drug
Labeler Name:
Medinatura
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
  • Intra-articular - Administration within a joint.
  • Intradermal - Administration within the dermis.
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • .ALPHA.-LIPOIC ACID 8 [hp_X]/2mL
  • ARNICA MONTANA ROOT 4 [hp_X]/2mL
  • COENZYME A 8 [hp_X]/2mL
  • COMFREY ROOT 6 [hp_X]/2mL
  • NADIDE 8 [hp_X]/2mL
  • SANGUINARIA CANADENSIS ROOT 4 [hp_X]/2mL
  • SODIUM DIETHYL OXALACETATE 8 [hp_X]/2mL
  • SOLANUM DULCAMARA TOP 3 [hp_X]/2mL
  • SULFUR 6 [hp_X]/2mL
  • SUS SCROFA CARTILAGE 6 [hp_X]/2mL
  • SUS SCROFA EMBRYO 6 [hp_X]/2mL
  • SUS SCROFA PLACENTA 6 [hp_X]/2mL
  • SUS SCROFA UMBILICAL CORD 6 [hp_X]/2mL
  • TOXICODENDRON PUBESCENS LEAF 2 [hp_X]/2mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    07-31-2014
    End Marketing 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
    50114-7030-110 AMPULE in 1 CARTON / 2 mL in 1 AMPULE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50114-7030-2?

    The NDC Packaged Code 50114-7030-2 is assigned to a package of 3 ampule in 1 carton / 2 ml in 1 ampule of Zeel, a human prescription drug labeled by Medinatura. The product's dosage form is injection and is administered via intra-articular; intradermal; intramuscular; intravenous; subcutaneous form.

    Is NDC 50114-7030 included in the NDC Directory?

    Yes, Zeel with product code 50114-7030 is active and included in the NDC Directory. The product was first marketed by Medinatura on July 31, 2014.

    What is the 11-digit format for NDC 50114-7030-2?

    The 11-digit format is 50114703002. 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
    5-4-150114-7030-25-4-250114-7030-02