Mds Roll-on Anti-perspirant Cream
NDC Package 87119-001-01

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

Package Information

Mds Roll-on Anti-perspirant (aluminum chlorohydrate) cream is apply to underarms only. This formulation utilizes a cream delivery system. Marketed by Mds Global Fze, this product is identified by NDC 87119-001 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
87119-001-01
Package Description
50 mL in 1 BOTTLE
Product Code
87119-001
11-Digit Billing Format
87119000101

Clinical Specifications

Proprietary Name
Mds Roll-on Anti-perspirant
Non-Proprietary Name
Aluminum Chlorohydrate
Substance Name
Aluminum Chlorohydrate Anhydrous
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)
ALUMINUM CHLOROHYDRATE ANHYDROUS 15.4 g/100mL
Usage Information
Apply to underarms only

Regulatory & Marketing

Labeler Name
Mds Global Fze
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-23-2025
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 87119-001-01 identifies a specific commercial package of 50 ml in 1 bottle of Mds Roll-on Anti-perspirant, a human over the counter drug labeled by Mds Global Fze. This cream is formulated for topical use and contains aluminum chlorohydrate anhydrous 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 Mds Global Fze on September 23, 2025. The current certification is valid through December 31, 2026.

How is this Mds Global Fze product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87119000101. 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)
87119-001-01
11-Digit CMS (5-4-2)
87119-0001-01

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