Geovita NDC 66343-116

NDC codes

FDA NDC Directory

Product NDC (as listed)66343-116Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66343-0116Add 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
66343-116-60	66343011660	60 mL in 1 BOTTLE (66343-116-60)Marketed from Dec 27, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Geovita
Generic name (nonproprietary): cerebrum, cuprum met, ferrum met, formicum acidum, silicea
Active ingredients: Sus scrofa cerebrum — 21 [hp_X]/60mLCopper — 21 [hp_X]/60mLIron — 6 [hp_X]/60mLFormic acid — 21 [hp_X]/60mLSilicon dioxide — 12 [hp_X]/60mL
Dosage form: Liquid
Route: Oral
Labeler: RUBIMED AG
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 27, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 66343-116_28179170-9016-61fc-e063-6394a90a8c64SPL ID 28179170-9016-61fc-e063-6394a90a8c64SPL set ID 0fcb5c06-d414-456c-a0ef-28e14018a781UNII 4GB5DQR532, 789U1901C5, E1UOL152H7, 0YIW783RG1, ETJ7Z6XBU4
Pharmacologic class: Copper-containing Intrauterine Device

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

N466343011660 followed by a unit qualifier and the quantity

Package 66343-0116-60. 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 Nov 29, 2024.

Indications (excerpt from the label)

Uses: (†) Homeopathic remedy for persons surrounded by electrosmog.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)