Muscle Ease NDC 55714-2487

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2487Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2487Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
55714-2487-1	55714248701	30 mL in 1 BOTTLE, GLASS (55714-2487-1)Marketed from Jan 1, 2019

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Muscle Ease
Generic name (nonproprietary): 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.
Active ingredients: Comfrey root — 6 [hp_X]/mLAconitum napellus — 15 [hp_X]/mLAntimony potassium tartrate — 15 [hp_X]/mLSilver nitrite — 15 [hp_X]/mLArnica montana — 15 [hp_X]/mLBryonia alba root — 15 [hp_X]/mLChelidonium majus — 15 [hp_X]/mLBlack cohosh — 15 [hp_X]/mLEupatorium perfoliatum flowering top — 15 [hp_X]/mLMatricaria chamomilla — 15 [hp_X]/mLStrychnos nux-vomica seed — 15 [hp_X]/mLToxicodendron pubescens leaf — 15 [hp_X]/mLRuta graveolens flowering top — 15 [hp_X]/mLLactic acid, L- — 15 [hp_X]/mLDatura stramonium — 15 [hp_X]/mLStrychnine — 15 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLHypericum perforatum — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 55714-2487_2d951f69-4225-5b39-e063-6394a90aa2e9SPL ID 2d951f69-4225-5b39-e063-6394a90aa2e9SPL set ID 9c5a4018-0230-e92b-e053-2995a90a4016UNII M9VVZ08EKQ, U0NQ8555JD, DL6OZ476V3, T3MZ57OGIF, O80TY208ZW, T7J046YI2B, 7E889U5RNN, K73E24S6X9, 1W0775VX6E, G0R4UBI2ZZ, 269XH13919, 6IO182RP7A, N94C2U587S, F9S9FFU82N, G6W4F0V8Z3, H9Y79VD43J, 11E6VI8VEG, XK4IUX8MNB
Pharmacologic class: Non-Standardized Plant Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N455714248701 followed by a unit qualifier and the quantity

Package 55714-2487-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Feb 7, 2025.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for associated symptoms such as bruising, pain, soreness, stiffness, spasms and weakness..

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)