NDC Package 55714-2487-1 Muscle Ease

Chamomilla,Phytolacca Decandra,Ruta Graveolens,Symphytum Officinale,Aconitum - 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:
55714-2487-1
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
Proprietary Name:
Muscle Ease
Non-Proprietary Name:
Chamomilla, Phytolacca Decandra, Ruta Graveolens, Symphytum Officinale, Aconitum Napellus, Antimonium Tartaricum, Argentum Nitricum, Arnica Montana, Bryonia, Chamomilla, Chelidonium Majus, Cimicifuga Racemosa, Eupatorium Perfoliatum, Hypericum Perforatum, Nux Vomica, Rhus Toxicodendron, Ruta Graveolens, Sarcolacticum Acidum, Stramonium, Strychninum.
Substance Name:
Aconitum Napellus; Antimony Potassium Tartrate; Arnica Montana; Black Cohosh; Bryonia Alba Root; Chelidonium Majus; Comfrey Root; Datura Stramonium; Eupatorium Perfoliatum Flowering Top; Hypericum Perforatum; Lactic Acid, L-; Matricaria Chamomilla; Phytolacca Americana Root; Ruta Graveolens Flowering Top; Silver Nitrite; Strychnine; Strychnos Nux-vomica Seed; Toxicodendron Pubescens Leaf
Usage Information:
Formulated for associated symptoms such as bruising, pain, soreness, stiffness, spasms and weakness..
11-Digit NDC Billing Format:
55714248701
Product Type:
Human Otc Drug
Labeler Name:
Newton Laboratories, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-01-2019
    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 55714-2487-1?

    The NDC Packaged Code 55714-2487-1 is assigned to a package of 30 ml in 1 bottle, glass of Muscle Ease, a human over the counter drug labeled by Newton Laboratories, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 55714-2487 included in the NDC Directory?

    Yes, Muscle Ease with product code 55714-2487 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on January 01, 2019 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 55714-2487-1?

    The 11-digit format is 55714248701. 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
    5-4-155714-2487-15-4-255714-2487-01