Agaricus Phosphorus NDC 48951-1022

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-1022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-1022Add 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
48951-1022-1	48951102201	10 AMPULE in 1 BOX (48951-1022-1) / 1 mL in 1 AMPULEMarketed 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): Agaricus Phosphorus
Generic name (nonproprietary): agaricus phosphorus
Active ingredients: Dryopteris filix-mas root — 3 [hp_X]/mLSilver fluoride — 6 [hp_X]/mLOstrea edulis shell — 6 [hp_X]/mLPhosphorus — 6 [hp_X]/mLAmanita muscaria fruiting body — 8 [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
Identifiers: Product ID 48951-1022_44210514-6a82-7a7f-e063-6394a90ae413SPL ID 44210514-6a82-7a7f-e063-6394a90ae413SPL set ID b6431e0b-6d84-423f-a1be-6701aa848f8dUNII C0ZK0RRF5X, 1Z00ZK3E66, 49OY13BE7Z, 27YLU75U4W, DIF093I037

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

N448951102201 followed by a unit qualifier and the quantity

Package 48951-1022-01. 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 Nov 21, 2025.

Indications (excerpt from the label)

FOR ORAL USE ONLY

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)