HZ-Chord NDC 64578-0065

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0065Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0065Add 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
64578-0065-1	64578006501	59.1 mL in 1 BOTTLE, DROPPER (64578-0065-1)Marketed from Sep 5, 2014

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): HZ-Chord
Generic name (nonproprietary): baptisia tinctoria, ceanothus americanus, citricum acidum, echinacea (angustifolia), gelsemium sempervirens, hydrocotyle asiatica, lycopodium clavatum, mercurius solubilis, mezereum, morbillinum, nux vomica, paloondo, phytolacca decandra, sepia, thuja occidentalis, thyroidinum (bovine)
Active ingredients: Baptisia tinctoria root — 4 [hp_X]/mLCeanothus americanus leaf — 6 [hp_X]/mLAnhydrous citric acid — 12 [hp_X]/mLEchinacea angustifolia — 4 [hp_X]/mLGelsemium sempervirens root — 12 [hp_X]/mLCentella asiatica — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLDaphne mezereum bark — 12 [hp_X]/mLMeasles virus — 30 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLLarrea tridentata top — 5 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLThyroid, Bovine — 9 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 5, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Allergens (Chemical structure)Calcium Chelating Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Decreased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 64578-0065_462ba065-76a7-0a0b-e063-6294a90a654dSPL ID 462ba065-76a7-0a0b-e063-6294a90a654dSPL set ID 9685aec5-a65d-40fe-b5d7-2f13a69733bcUNII 5EF0HWI5WU, 25B1Y14T8N, XF417D3PSL, VB06AV5US8, 639KR60Q1Q, 7M867G6T1U, C88X29Y479, 324Y4038G2, X2N6E405GV, HT3R7C012Q, 269XH13919, PK0TXD049P, 11E6VI8VEG, QDL83WN8C2, 1NT28V9397, MN18OTN73W
Pharmacologic class: Anti-coagulant; Calculi Dissolution 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

N464578006501 followed by a unit qualifier and the quantity

Package 64578-0065-01. 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 Dec 17, 2025.

Indications (excerpt from the label)

Purpose Temporary relief of itching skin eruptions, warts, canker sores.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)