Magnesium phosphoricum 6X NDC 48951-7220

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-7220Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-7220Add 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
48951-7220-4	48951722004	50 g in 1 BOTTLE, GLASS (48951-7220-4)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): Magnesium phosphoricum 6X
Generic name (nonproprietary): magnesium phosphoricum 6x
Active ingredients: Magnesium phosphate — 6 [hp_X]/g
Dosage form: Powder
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: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 48951-7220_36eb354c-9178-0d49-e063-6294a90ab28dSPL ID 36eb354c-9178-0d49-e063-6294a90ab28dSPL set ID 36eb354c-9177-0d49-e063-6294a90ab28dUNII 453COF7817
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N448951722004 followed by a unit qualifier and the quantity

Package 48951-7220-04. 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 Jun 6, 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)