Aurum Met (aurum metallicum) NDC 44911-0380

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0380Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0380Add 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
44911-0380-1	44911038001	30 mL in 1 BOTTLE, DROPPER (44911-0380-1)Marketed from Aug 16, 2016

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): Aurum Met
Generic name (nonproprietary): aurum metallicum
Active ingredients: Gold — 200 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 16, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 44911-0380_27858e7d-6b7a-4f67-9f94-22a6d4a995d9SPL ID 27858e7d-6b7a-4f67-9f94-22a6d4a995d9SPL set ID 9d7de1b6-8d5e-4881-9511-4723736a5abfUNII 79Y1949PYOUPC 0363113600445
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

N444911038001 followed by a unit qualifier and the quantity

Package 44911-0380-01. 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 Sep 23, 2024.

Indications (excerpt from the label)

USES: May temporarily relieve: •melancholy •hopelessness** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)