Neuro-Chord (homeopathic liquid) NDC 64578-0180

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0180Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0180Add 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
64578-0180-1	64578018001	59.1 mL in 1 BOTTLE, DROPPER (64578-0180-1)Marketed from Nov 3, 2017

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): Neuro-Chord
Generic name (nonproprietary): homeopathic liquid
Active ingredients: Gelsemium sempervirens root — 30 [hp_X]/59.1mLSus scrofa adrenal gland — 9 [hp_X]/59.1mLLatrodectus mactans — 30 [hp_X]/59.1mLNaja naja venom — 30 [hp_X]/59.1mLPhosphorus — 12 [hp_X]/59.1mLLead — 15 [hp_X]/59.1mLPyridoxine hydrochloride — 12 [hp_X]/59.1mLToxicodendron pubescens leaf — 12 [hp_X]/59.1mLRiboflavin — 12 [hp_X]/59.1mLSarsaparilla — 6 [hp_X]/59.1mLThiamine hydrochloride — 12 [hp_X]/59.1mLZinc — 15 [hp_X]/59.1mLAmanita muscaria fruiting body — 12 [hp_X]/59.1mLAluminum — 15 [hp_X]/59.1mLArsenic — 15 [hp_X]/59.1mLCadmium — 15 [hp_X]/59.1mLCoenzyme a — 12 [hp_X]/59.1mLConium maculatum flowering top — 12 [hp_X]/59.1mLCopper — 15 [hp_X]/59.1mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 3, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Analogs/Derivatives (Chemical/Ingredient)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Vitamin B 6 (Chemical/Ingredient)
Identifiers: Product ID 64578-0180_58ca4615-3880-6c1f-e063-6394a90a8924SPL ID 58ca4615-3880-6c1f-e063-6394a90a8924SPL set ID 462c21ba-7304-3606-e063-6294a90aab21UNII 639KR60Q1Q, 398IYQ16YV, XJJ7QA858R, ZZ4AG7L7VM, 27YLU75U4W, 2P299V784P, 68Y4CF58BV, 6IO182RP7A, TLM2976OFR, 2H1576D5WG, M572600E5P, J41CSQ7QDS, DIF093I037, CPD4NFA903, N712M78A8G, 00BH33GNGH, SAA04E81UX, Q28R5GF371, 789U1901C5
Pharmacologic class: Copper-containing Intrauterine Device; Vitamin B6 Analog

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

N464578018001 followed by a unit qualifier and the quantity

Package 64578-0180-01. 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 Aug 11, 2026.

Indications (excerpt from the label)

Uses Temporary relief of ocassional numbness, irritability, tingling.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)