Muscle Ease

Manufacturer
Newton Laboratories, Inc.
Effective date
2025-02-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:31:52

Label at a glance#

ProductMuscle Ease
Active ingredientCOMFREY ROOT, ACONITUM NAPELLUS, ANTIMONY POTASSIUM TARTRATE, SILVER NITRITE, ARNICA MONTANA, BRYONIA ALBA ROOT, CHELIDONIUM MAJUS, BLACK COHOSH, EUPATORIUM PERFOLIATUM FLOWERING TOP, MATRICARIA CHAMOMILLA, STRYCHNOS NUX-VOMICA SEED, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, LACTIC ACID, L-, DATURA STRAMONIUM, STRYCHNINE, PHYTOLACCA AMERICANA ROOT, HYPERICUM PERFORATUM
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) as needed or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Chamomilla 6x, Phytolacca decandra 6x, Ruta graveolens 6x, Symphytum officinale 6x, Aconitum napellus 15x, Antimonium tartaricum 15x, Argentum nitricum 15x, Arnica montana 15x, Bryonia 15x, Chamomilla 15x, Chelidonium majus 15x, Cimicifuga racemosa 15x, Eupatorium perfoliatum 15x, Hypericum perforatum 15x, Nux vomica 15x, Rhus toxicodendron 15x, Ruta graveolens 15x, Sarcolacticum acidum 15x, Stramonium 15x, Strychninum 15

OTC - PURPOSE SECTION

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

INACTIVE INGREDIENT SECTION

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

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net – Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-2487-1Muscle Ease30 mL in 1 BOTTLE, GLASSLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-2487MUSCLE EASE (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.) LIQUID [NEWTON LABORATORIES, INC.]3Current NDC, Legacy NDC, 1 package rows20250210_9c5a4018-0230-e92b-e053-2995a90a4016.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-248755714-2487-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Muscle EaseCHAMOMILLA, 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.Newton Laboratories, Inc.9c5a4018-0230-e92b-e053-2995a90a40162025-02-07WarningsExact identifier
ndc (package): 55714-2487-1
ndc (product): 55714-2487
ndc11 (package): 55714248701
spl id: 2d951f69-4225-5b39-e063-6394a90aa2e9
spl set id: 9c5a4018-0230-e92b-e053-2995a90a4016

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.