Ferrodonna NDC 59469-122

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-122Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0122Add 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
59469-122-10	59469012210	1 BOTTLE, GLASS in 1 BOX (59469-122-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Apr 12, 2008

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): Ferrodonna
Generic name (nonproprietary): arsenic trioxide, ceanothus americanus leaf, cinchona officinalis bark, cobaltous nitrate, cupric sulfate, iron, manganese acetate, and sodium chloride
Active ingredients: Arsenic trioxide — 12 [hp_X]/50mLCeanothus americanus leaf — 5 [hp_X]/50mLCinchona officinalis bark — 4 [hp_X]/50mLCobaltous nitrate — 6 [hp_X]/50mLCupric sulfate — 6 [hp_X]/50mLIron — 12 [hp_X]/50mLManganese acetate — 6 [hp_X]/50mLSodium chloride — 12 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 12, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 59469-122_5b96c654-6f25-43f0-b240-a1502fefc009SPL ID 5b96c654-6f25-43f0-b240-a1502fefc009SPL set ID 64c6f75a-382d-4aa0-b210-6be83a62fa3fUNII S7V92P67HO, 25B1Y14T8N, S003A158SB, 65W79BFD5V, LRX7AJ16DT, E1UOL152H7, 0V6E9Q2I0Y, 451W47IQ8X
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

N459469012210 followed by a unit qualifier and the quantity

Package 59469-0122-10. 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 14, 2022.

Indications (excerpt from the label)

Indications For relief of minor occasional weakness. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)