Nervionix Pro Magnesium Ice Cream
NDC Package 87752-003-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Nervionix Pro Magnesium Ice (lidocaine hydrochloride, menthol, magnesium chloride) cream is adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily.Children under 12 years of age: Consult a doctor before use.We recommend testing a small amount of cream on your skin first to check for skin reaction and comfort level; wait 15 minutes before applying to affected area if you are happy with the comfort level. This formulation utilizes a cream delivery system. Marketed by Micelle Laboratories, Incorporated, this product is identified by NDC 87752-003.

Identification & Billing

NDC Package Code
87752-003-01
Package Description
240 mL in 1 JAR
Product Code
87752-003
11-Digit Billing Format
87752000301

Clinical Specifications

Proprietary Name
Nervionix Pro Magnesium Ice
Non-Proprietary Name
Lidocaine Hydrochloride, Menthol, Magnesium Chloride
Substance Name
Lidocaine Hydrochloride; Menthol; Magnesium Chloride
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily.Children under 12 years of age: Consult a doctor before use.We recommend testing a small amount of cream on your skin first to check for skin reaction and comfort level; wait 15 minutes before applying to affected area if you are happy with the comfort level.

Regulatory & Marketing

Labeler Name
Micelle Laboratories, Incorporated
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
06-25-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 87752-003-01 identifies a specific commercial package of 240 ml in 1 jar of Nervionix Pro Magnesium Ice, a human over the counter drug labeled by Micelle Laboratories, Incorporated. This cream is formulated for topical use and contains lidocaine hydrochloride; menthol; magnesium chloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Micelle Laboratories, Incorporated on June 25, 2026. The current certification is valid through December 31, 2027.

How is this Micelle Laboratories, Incorporated product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87752000301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
87752-003-01
11-Digit CMS (5-4-2)
87752-0003-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.