NDC Package 51885-9489-8 Zeel

Alpha Lipoic Acid,Arnica Montana Whole, Sus Scrofa Cartilage,Coenzyme A, Solanum Dulcamara - 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:
51885-9489-8
Package Description:
1 TUBE in 1 CARTON / 100 g in 1 TUBE
Product Code:
Proprietary Name:
Zeel
Non-Proprietary Name:
Alpha Lipoic Acid, Arnica Montana Whole, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Silicon Dioxide, Sulfur, Coriander
Substance Name:
Alpha Lipoic Acid; Arnica Montana Whole; Coenzyme A; Coriander; Nadide; Sanguinaria Canadensis Root; Silicon Dioxide; 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:
Directions: Adults: Apply generously to affected areas2 to 3 times daily, or as directed by your health professional.Massage thoroughly into skin. Children under 18 yearsof age: consult your healthcare professional.Indications: For the temporary relief of minor arthritispain and joint stiffness
11-Digit NDC Billing Format:
51885948908
Product Type:
Human Otc Drug
Labeler Name:
Biologische Heilmittel Heel
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):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    09-22-2021
    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 51885-9489-8?

    The NDC Packaged Code 51885-9489-8 is assigned to a package of 1 tube in 1 carton / 100 g in 1 tube of Zeel, a human over the counter drug labeled by Biologische Heilmittel Heel. The product's dosage form is ointment and is administered via topical form.

    Is NDC 51885-9489 included in the NDC Directory?

    Yes, Zeel with product code 51885-9489 is active and included in the NDC Directory. The product was first marketed by Biologische Heilmittel Heel on September 22, 2021 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 51885-9489-8?

    The 11-digit format is 51885948908. 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
    5-4-151885-9489-85-4-251885-9489-08