Sciatica-Nerve Care NDC 55714-2513

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2513Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2513Add 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
55714-2513-1	55714251301	28 g in 1 BOTTLE, GLASS (55714-2513-1)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): Sciatica-Nerve Care
Generic name (nonproprietary): aconitum nap., ammonium benzoicum, arsenicum alb., benzoicum acidum, bryonia, causticum, cinchona, colchicum, gnaphalium polycephalum, iris versicolor, kali iod., ledum, lithium carb., nux vom., phytolacca, rhus toxicoderon, ruta, sambucus nig., strychninum, hypericum, urtica ur
Active ingredients: Aconitum napellus — 15 [hp_X]/gAmmonium benzoate — 15 [hp_X]/gArsenic trioxide — 15 [hp_X]/gBenzoic acid — 15 [hp_X]/gBryonia alba root — 15 [hp_X]/gCausticum — 15 [hp_X]/gCinchona officinalis bark — 15 [hp_X]/gColchicum autumnale bulb — 15 [hp_X]/gPseudognaphalium obtusifolium — 15 [hp_X]/gIris versicolor root — 15 [hp_X]/gPotassium iodide — 15 [hp_X]/gRhododendron tomentosum leafy twig — 15 [hp_X]/gLithium carbonate — 15 [hp_X]/gStrychnos nux-vomica seed — 15 [hp_X]/gPhytolacca americana root — 15 [hp_X]/gToxicodendron pubescens leaf — 15 [hp_X]/gRuta graveolens flowering top — 15 [hp_X]/gSambucus nigra flowering top — 15 [hp_X]/gStrychnine — 15 [hp_X]/gHypericum perforatum — 6 [hp_X]/gUrtica urens — 6 [hp_X]/g
Dosage form: Pellet
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)Ammonium Ion Binding Activity (Mechanism)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 55714-2513_2dcfec4c-76f4-0efd-e063-6394a90acdf6SPL ID 2dcfec4c-76f4-0efd-e063-6394a90acdf6SPL set ID 9cbda496-ef30-18af-e053-2995a90a2321UNII U0NQ8555JD, AC80WD7GPF, S7V92P67HO, 8SKN0B0MIM, T7J046YI2B, DD5FO1WKFU, S003A158SB, 993QHL78E6, 36XQ854NWW, X43D4L3DQC, 1C4QK22F9J, 877L01IZ0P, 2BMD2GNA4V, 269XH13919, 11E6VI8VEG, 6IO182RP7A, N94C2U587S, CT03BSA18U, H9Y79VD43J, XK4IUX8MNB, IHN2NQ5OF9
Pharmacologic class: Mood Stabilizer; Nitrogen Binding Agent; 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

N455714251301 followed by a unit qualifier and the quantity

Package 55714-2513-01. 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 10, 2025.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for associated symptoms such as sharp or throbbing pain, Inflammation, numbness and discomfort.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)