Mag Phos (magnesia phosphorica) NDC 44911-0353

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0353Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0353Add 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
44911-0353-1	44911035301	30 mL in 1 BOTTLE, DROPPER (44911-0353-1)Marketed from Apr 20, 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): Mag Phos
Generic name (nonproprietary): magnesia phosphorica
Active ingredients: Magnesium phosphate, Dibasic trihydrate — 30 [hp_C]/30mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 20, 2016
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 44911-0353_98f47b41-555c-491a-9ed2-5c7311731809SPL ID 98f47b41-555c-491a-9ed2-5c7311731809SPL set ID c0fbff46-a75c-48d2-bfb2-ef3484c318a4UNII HF539G9L3Q
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

N444911035301 followed by a unit qualifier and the quantity

Package 44911-0353-01. 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 14, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve nerve pain and cramping pain.** **Clains 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)