Magnesia Phosphorica NDC 71753-8008

NDC codes

FDA NDC Directory

Product NDC (as listed)71753-8008Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71753-8008Add 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
71753-8008-1	71753800801	30 mL in 1 BOTTLE, SPRAY (71753-8008-1)Marketed from Sep 30, 2020

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): Magnesia Phosphorica
Generic name (nonproprietary): magnesia phosphorica
Active ingredients: Magnesium phosphate, Dibasic trihydrate — 12 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Ratis, LLC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 30, 2020
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 71753-8008_9b278f18-f2f7-4cf3-991e-34caa8ace79cSPL ID 9b278f18-f2f7-4cf3-991e-34caa8ace79cSPL set ID ba728942-4fa1-434e-9d94-be313c40e7d7UNII HF539G9L3QUPC 0371753800811
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

N471753800801 followed by a unit qualifier and the quantity

Package 71753-8008-01. 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 May 17, 2023.

Indications (excerpt from the label)

USES: May temporarily relieve pain, muscle cramps, menstrual cramps, headache, earache, toothache, and nerve injuries.* *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)