Aurum 20X NDC 48951-1392

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-1392Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-1392Add 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
48951-1392-3	48951139203	60 mL in 1 BOTTLE, DROPPER (48951-1392-3)Marketed from Sep 1, 2009

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 20X
Generic name (nonproprietary): aurum 20x
Active ingredients: Gold — 20 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Uriel Pharmacy, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2009
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 48951-1392_2c3eb1bf-24e8-eb25-e063-6294a90a4543SPL ID 2c3eb1bf-24e8-eb25-e063-6294a90a4543SPL set ID 2c3eb1bf-24e7-eb25-e063-6294a90a4543UNII 79Y1949PYO
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

N448951139203 followed by a unit qualifier and the quantity

Package 48951-1392-03. 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 21, 2025.

Indications (excerpt from the label)

Directions: FOR ORAL USE ONLY.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)