Nervionix Pro Magnesium Ice NDC 87752-003

NDC codes

FDA NDC Directory

Product NDC (as listed)87752-003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87752-0003Add 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
87752-003-01	87752000301	240 mL in 1 JAR (87752-003-01)Marketed from Jun 25, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Nervionix Pro Magnesium Ice
Generic name (nonproprietary): lidocaine hydrochloride, menthol,magnesium chloride
Active ingredients: Lidocaine hydrochloride — 1 g/100mLMenthol — 3.7 g/100mLMagnesium chloride — 2 g/100mL
Dosage form: Cream
Route: Topical
Labeler: Micelle Laboratories, Incorporated
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 25, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Amides (Chemical structure)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Local Anesthesia (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 87752-003_5631a520-7225-b6c8-e063-6294a90a1a87SPL ID 5631a520-7225-b6c8-e063-6294a90a1a87SPL set ID c11e0963-90fb-48c6-938a-3dcbbad17acaRxCUI 2747156UNII V13007Z41A, L7T10EIP3A, 02F3473H9O
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic; 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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N487752000301 followed by a unit qualifier and the quantity

Package 87752-0003-01. 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 Jul 9, 2026.

Indications (excerpt from the label)

Uses Soothing relief of pain, stiffness, tingling, or burning nerve pain associated with arthritis, muscles and joint pains, cramps and soreness, backache, and sciatica.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)