Nanoxtreme Pain Relieving Cream
NDC Package 84804-321-01

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

Package Information

Nanoxtreme Pain Relieving (menthol, methyl salicylate) cream is adults and children 2 years of age and older: Apply to affected areas not more than 3 to 4 times daily. This formulation utilizes a cream delivery system. Marketed by Mg Science Technologies Llc, this product is identified by NDC 84804-321 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
84804-321-01
Package Description
100 mL in 1 TUBE
Product Code
84804-321
11-Digit Billing Format
84804032101
RxNorm Crosswalk
  • RxCUI: 2698214 - menthol 4 % / methyl salicylate 10 % Topical Cream
  • RxCUI: 2698214 - menthol 40 MG/ML / methyl salicylate 100 MG/ML Topical Cream

Clinical Specifications

Proprietary Name
Nanoxtreme Pain Relieving
Non-Proprietary Name
Menthol, Methyl Salicylate
Substance Name
Menthol; Methyl Salicylate
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)
Usage Information
Adults and children 2 years of age and older: Apply to affected areas not more than 3 to 4 times daily. Children under 2 years of age: Do not use, consult a doctor.

Regulatory & Marketing

Labeler Name
Mg Science Technologies Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-23-2024
Listing Expiration
12-31-2026
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 84804-321-01 identifies a specific commercial package of 100 ml in 1 tube of Nanoxtreme Pain Relieving, a human over the counter drug labeled by Mg Science Technologies Llc. This cream is formulated for topical use and contains menthol; methyl salicylate 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 Mg Science Technologies Llc on November 23, 2024. The current certification is valid through December 31, 2026.

How is this Mg Science Technologies Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84804032101. 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)
84804-321-01
11-Digit CMS (5-4-2)
84804-0321-01

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