Gyne-Chord (homeopathic liquid) NDC 64578-0063

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0063Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0063Add 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
64578-0063-1	64578006301	59.1 mL in 1 BOTTLE, DROPPER (64578-0063-1)Marketed from Jul 19, 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): Gyne-Chord
Generic name (nonproprietary): homeopathic liquid
Active ingredients: Angelica sinensis root — 8 [hp_X]/59.1mLGold trichloride — 15 [hp_X]/59.1mLBoric acid — 12 [hp_X]/59.1mLOyster shell calcium carbonate, Crude — 15 [hp_X]/59.1mLCandida albicans — 12 [hp_X]/59.1mLBlack cohosh — 6 [hp_X]/59.1mLEstrone — 7 [hp_C]/59.1mLSus scrofa adrenal gland — 9 [hp_X]/59.1mLChamaelirium luteum root — 12 [hp_X]/59.1mLGoldenseal — 12 [hp_X]/59.1mLWood creosote — 15 [hp_X]/59.1mLMercurius solubilis — 12 [hp_X]/59.1mLSodium sulfate — 12 [hp_X]/59.1mLSus scrofa ovary — 9 [hp_X]/59.1mLPulsatilla vulgaris — 12 [hp_X]/59.1mLSepia officinalis juice — 12 [hp_X]/59.1mLDelphinium staphisagria seed — 12 [hp_X]/59.1mLThuja occidentalis leafy twig — 12 [hp_X]/59.1mLThyroid, Unspecified — 9 [hp_X]/59.1mLZinc gluconate — 8 [hp_X]/59.1mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 19, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 64578-0063_2903f2e4-a7f9-629f-e063-6294a90a318aSPL ID 2903f2e4-a7f9-629f-e063-6294a90a318aSPL set ID 2e9fda67-6bda-4bac-aec8-065f0bf58270UNII B66F4574UG, 15443PR153, R57ZHV85D4, 2E32821G6I, 4D7G21HDBC, K73E24S6X9, 2DI9HA706A, 398IYQ16YV, DQV54Y5H3U, ZW3Z11D0JV, 3JYG22FD73, 324Y4038G2, 0YPR65R21J, S7YTV04R8O, I76KB35JEV, QDL83WN8C2, 00543AP1JV, 1NT28V9397, 0B4FDL9I6P, U6WSN5SQ1Z
Pharmacologic class: Copper Absorption Inhibitor; Non-Standardized Fungal 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

N464578006301 followed by a unit qualifier and the quantity

Package 64578-0063-01. 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 11, 2024.

Indications (excerpt from the label)

Uses Temporary relief of vaginal discomfort, disrupted menses.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)