1. Labeler Index
  2. Newton Laboratories, Inc.
  3. NDC: 55714-2272 Muscle Ease

NDC 55714-2272 Muscle Ease

Aconitum Nap., Antimon. Tart.,arg. Nit., Arnica, Bryonia, Chamomilla,chelidonium Majus, Cimicifuga, Eupatorium Perf.,hypericum, Nux Vom., Rhus Toxicodendron, Ruta,sarcolacticum Ac., Stramonium, Strychninum,chamomilla, Phytolacca, Ruta, Symphytum.

NDC Product Code 55714-2272

NDC Code: 55714-2272

Proprietary Name: Muscle Ease What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Aconitum Nap., Antimon. Tart.,arg. Nit., Arnica, Bryonia, Chamomilla,chelidonium Majus, Cimicifuga, Eupatorium Perf.,hypericum, Nux Vom., Rhus Toxicodendron, Ruta,sarcolacticum Ac., Stramonium, Strychninum,chamomilla, Phytolacca, Ruta, Symphytum. What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Code Structure
  • 55714 - Newton Laboratories, Inc.
    • 55714-2272 - Muscle Ease

NDC 55714-2272-1

Package Description: 29.57 mL in 1 BOTTLE, GLASS

NDC 55714-2272-2

Package Description: 59.14 mL in 1 BOTTLE, GLASS

NDC Product Information

Muscle Ease with NDC 55714-2272 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Muscle Ease is aconitum nap., antimon. tart.,arg. nit., arnica, bryonia, chamomilla,chelidonium majus, cimicifuga, eupatorium perf.,hypericum, nux vom., rhus toxicodendron, ruta,sarcolacticum ac., stramonium, strychninum,chamomilla, phytolacca, ruta, symphytum.. The product's dosage form is liquid and is administered via oral form.

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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Muscle Ease Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
  • ACONITUM NAPELLUS 15 [hp_X]/mL
  • ANTIMONY POTASSIUM TARTRATE 15 [hp_X]/mL
  • SILVER NITRATE 15 [hp_X]/mL
  • ARNICA MONTANA 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • MATRICARIA RECUTITA 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • BLACK COHOSH 15 [hp_X]/mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 15 [hp_X]/mL
  • HYPERICUM PERFORATUM 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 15 [hp_X]/mL
  • RUTA GRAVEOLENS FLOWERING TOP 15 [hp_X]/mL
  • LACTIC ACID, L- 15 [hp_X]/mL
  • DATURA STRAMONIUM 15 [hp_X]/mL
  • STRYCHNINE 15 [hp_X]/mL
  • MATRICARIA RECUTITA 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • RUTA GRAVEOLENS FLOWERING TOP 3 [hp_X]/mL
  • COMFREY ROOT 3 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Newton Laboratories, Inc.
Labeler Code: 55714
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date: 03-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: E What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Muscle Ease Product Label Images

Muscle Ease Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage Section

Muscle Ease  Formulated for symptoms associated with muscle discomfort such as bruising, pain, soreness, stiffness, spasms and weakness.

Dosage & Administration Section

Directions: ORAL USE ONLY - SHAKE WELL.  Ages 12 and up, take 6 drops orally (ages 0 to 11, give 3 drops) as needed or as directed by a healthcare professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

Otc - Active Ingredient Section

Aconitum nap. 15x, Antimon. tart. 15x, Arg. nit. 15x, Arnica 15x, Bryonia 15x, Chamomilla 15x, Chelidonium majus 15x, Cimicifuga 15x, Eupatorium perf. 15x, Hypericum 15x, Nux vom. 15x, Rhus toxicodendron 15x, Ruta 15x,Sarcolacticum ac. 15x, Stramonium 15x, Strychninum 15x, Chamomilla 3x, Phytolacca 3x, Ruta 3x, Symphytum 3x.

Otc - Purpose Section

Formulated for symptoms associated with muscle discomfort such as bruising, pain, soreness, stiffness, spasms and weakness.

Inactive Ingredient Section

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.

Questions Section

Www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012Questions?  1.800.448.7256

Warnings Section

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children

Otc - Pregnancy Or Breast Feeding Section

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children

* Please review the disclaimer below.

Previous Code
55714-2271
Next Code
55714-2273