Nivexis Dmso Multi-relief Repair Cream
NDC Package 83091-003-01

11-digit billing NDC: 83091000301
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Nivexis Dmso Multi-relief Repair Cream (dmso multi-relief repair cream) cream is rub the affected area with warm water and pat dry thoroughly,ensuring the skin is free of oil, dust, or sweat; evenly apply it tothe painful area, gently massage for 1-2 minutes until absorbed. This formulation utilizes a cream delivery system. Marketed by Anhui Grass Coral Biotechnology Co., Ltd, this product is identified by NDC 83091-003 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
83091-003-01
Package Description
118 mL in 1 BOTTLE
Product Code
83091-003
11-Digit Billing Format
83091000301

Clinical Specifications

Proprietary Name
Nivexis Dmso Multi-relief Repair Cream
Non-Proprietary Name
Dmso Multi-relief Repair Cream
Substance Name
Menthol
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)
MENTHOL 2 g/100mL
Usage Information
Rub the affected area with warm water and pat dry thoroughly,ensuring the skin is free of oil, dust, or sweat; evenly apply it tothe painful area, gently massage for 1-2 minutes until absorbed.

Regulatory & Marketing

Labeler Name
Anhui Grass Coral Biotechnology Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-30-2026
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 83091-003-01 identifies a specific commercial package of 118 ml in 1 bottle of Nivexis Dmso Multi-relief Repair Cream, a human over the counter drug labeled by Anhui Grass Coral Biotechnology Co., Ltd. This cream is formulated for topical use and contains menthol 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 Anhui Grass Coral Biotechnology Co., Ltd on September 30, 2026. The current certification is valid through December 31, 2027.

How is this Anhui Grass Coral Biotechnology Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83091000301. 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)
83091-003-01
11-Digit CMS (5-4-2)
83091-0003-01

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