Medi-Chord (homeopathic liquid) NDC 64578-0060

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0060Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0060Add 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
64578-0060-1	64578006001	59.1 mL in 1 BOTTLE, DROPPER (64578-0060-1)Marketed from Sep 21, 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): Medi-Chord
Generic name (nonproprietary): homeopathic liquid
Active ingredients: Acetic acid — 18 [hp_X]/59.1mLAspirin — 18 [hp_X]/59.1mLCorticotropin human — 18 [hp_X]/59.1mLAluminum — 18 [hp_X]/59.1mLAtropa belladonna — 12 [hp_X]/59.1mLBenzene — 12 [hp_X]/59.1mLChloramphenicol — 18 [hp_X]/59.1mLChlorpromazine — 18 [hp_X]/59.1mLCortisone acetate — 18 [hp_X]/59.1mLEstrone — 18 [hp_X]/59.1mLSus scrofa adrenal gland — 9 [hp_X]/59.1mLGlycyrrhiza glabra — 4 [hp_X]/59.1mLPork liver — 9 [hp_X]/59.1mLPotassium iodide — 12 [hp_X]/59.1mLArctium lappa root — 4 [hp_X]/59.1mLLycopodium clavatum spore — 12 [hp_X]/59.1mLNitric acid — 12 [hp_X]/59.1mLStrychnos nux-vomica seed — 12 [hp_X]/59.1mLKerosene — 18 [hp_X]/59.1mLPhenacetin — 18 [hp_X]/59.1mLPhosphoric acid — 12 [hp_X]/59.1mLPhytolacca americana root — 4 [hp_X]/59.1mLLead — 15 [hp_X]/59.1mLFrangula purshiana bark — 4 [hp_X]/59.1mLPhenyl salicylate — 18 [hp_X]/59.1mLSarsaparilla — 4 [hp_X]/59.1mLThyroid, Unspecified — 9 [hp_X]/59.1mLTrifolium pratense flower — 4 [hp_X]/59.1mLElymus repens root — 4 [hp_X]/59.1mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 21, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Amphenicols (EXT)Non-Steroidal (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Corticosteroid Hormone Receptor Agonists (Mechanism)Cyclooxygenase Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)Decreased Prostaglandin Production (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Phenothiazines (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 64578-0060_58c9adf5-1117-f8da-e063-6394a90a6d4dSPL ID 58c9adf5-1117-f8da-e063-6394a90a6d4dSPL set ID 57bc618b-15bd-4d04-8037-fb192e743e30UNII Q40Q9N063P, R16CO5Y76E, 63KF469V7T, CPD4NFA903, WQZ3G9PF0H, J64922108F, 66974FR9Q1, U42B7VYA4P, 883WKN7W8X, 2DI9HA706A, 398IYQ16YV, 2788Z9758H, 6EC706HI7F, 1C4QK22F9J, 597E9BI3Z3, C88X29Y479, 411VRN1TV4, 269XH13919, 1C89KKC04E, ER0CTH01H9, E4GA8884NN, 11E6VI8VEG, 2P299V784P, 4VBP01X99F, 28A37T47QO, 2H1576D5WG, 0B4FDL9I6P, 4JS0838828, 3IXW0F6P8W
Pharmacologic class: Amphenicol-class Antibacterial; Corticosteroid; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Nonsteroidal Anti-inflammatory Drug; Phenothiazine; Platelet Aggregation Inhibitor

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

N464578006001 followed by a unit qualifier and the quantity

Package 64578-0060-01. 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 headache, joint pain, skin eruption, itching.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)