Chavita 4 NDC 66343-085

NDC codes

FDA NDC Directory

Product NDC (as listed)66343-085Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66343-0085Add 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
66343-085-60	66343008560	60 mL in 1 BOTTLE (66343-085-60)Marketed from Dec 19, 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): Chavita 4
Generic name (nonproprietary): aur met, crataegus, cetraria, eucalyptus globulus, ferrum met, thymus gland, zinc val
Active ingredients: Gold — 21 [hp_X]/60mLHawthorn leaf with flower — 21 [hp_X]/60mLCetraria islandica whole — 21 [hp_X]/60mLEucalyptus globulus leaf — 21 [hp_X]/60mLIron — 50 [hp_C]/60mLBos taurus thymus — 21 [hp_X]/60mLZinc valerate dihydrate — 200 [hp_C]/60mL
Dosage form: Liquid
Route: Oral
Labeler: RUBIMED AG
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 66343-085_2817e573-e0e2-d03c-e063-6394a90afb9eSPL ID 2817e573-e0e2-d03c-e063-6394a90afb9eSPL set ID c0cf6f37-6f96-4126-ae8c-12c89a77e02eUNII 79Y1949PYO, 6OM09RPY36, BJ7YPN79A1, S546YLW6E6, E1UOL152H7, 8XEJ88V2T8, MN0RX54EQA
Pharmacologic class: Standardized Chemical Allergen

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

N466343008560 followed by a unit qualifier and the quantity

Package 66343-0085-60. 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 Oct 29, 2024.

Indications (excerpt from the label)

Uses: (†) Homeopathic remedy for hay fever and allergies.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)