What is NDC 59469-324?

59469-324 is the product NDC for Cardinorma, Arnica montana root 4 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Cardinorma (Arnica montana Root, Activated Charcoal, Potassium carbonate, Lachesis Muta Venom, Nerium oleander Leaf, Tobacco Leaf, Peumus boldus Leaf, and SELENICEREUS GRANDIFLORUS WHOLE).

What is the active ingredient?

Arnica montana root, Activated charcoal, Potassium carbonate, Lachesis muta venom, Nerium oleander leaf, Tobacco leaf, Peumus boldus leaf, Selenicereus grandiflorus whole.

PEKANA Naturheilmittel GmbH, NDC labeler code 59469. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Cardinorma?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cardinorma NDC 59469-324 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-324Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0324Add 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
59469-324-10	5946903241059469032410	1 BOTTLE, GLASS in 1 BOX (59469-324-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Jun 24, 2019

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): Cardinorma
Generic name (nonproprietary): arnica montana root, activated charcoal, potassium carbonate, lachesis muta venom, nerium oleander leaf, tobacco leaf, peumus boldus leaf, and selenicereus grandiflorus whole
Active ingredients: Arnica montana root — 4 [hp_X]/50mLActivated charcoal — 8 [hp_X]/50mLPotassium carbonate — 4 [hp_X]/50mLLachesis muta venom — 8 [hp_X]/50mLNerium oleander leaf — 4 [hp_X]/50mLTobacco leaf — 6 [hp_X]/50mLPeumus boldus leaf — 4 [hp_X]/50mLSelenicereus grandiflorus whole — 4 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbHNDC labeler code 59469
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 24, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 59469-324_ee10404e-1016-4ab0-a62e-fa8c54a39f3bSPL ID ee10404e-1016-4ab0-a62e-fa8c54a39f3bSPL set ID d84eabc6-c17b-41b9-a450-5ebc0752ca03UNII MUE8Y11327, 2P3VWU3H10, BQN1B9B9HA, VSW71SS07I, 7KV510R6H6, 6YR2608RSU, Q4EWM09M3O, X8H7HS7MRM
Pharmacologic class: Non-Standardized Plant 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

N459469032410 followed by a unit qualifier and the quantity

Package 59469-0324-10. 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 Jan 11, 2023.

Indications (excerpt from the label)

Indications For occasional tiredness often experienced by the elderly. 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)

About NDC 59469-324

What is NDC 59469-324?: 59469-324 is the product NDC for Cardinorma, Arnica montana root 4 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cardinorma (Arnica montana Root, Activated Charcoal, Potassium carbonate, Lachesis Muta Venom, Nerium oleander Leaf, Tobacco Leaf, Peumus boldus Leaf, and SELENICEREUS GRANDIFLORUS WHOLE).
What is the active ingredient?: Arnica montana root, Activated charcoal, Potassium carbonate, Lachesis muta venom, Nerium oleander leaf, Tobacco leaf, Peumus boldus leaf, Selenicereus grandiflorus whole.
Who is the labeler?: PEKANA Naturheilmittel GmbH, NDC labeler code 59469. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cardinorma?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.