Oxy Face Wash
NDC Package 10742-8397-2

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Oxy Face Wash is a . Marketed by The Mentholatum Company, this product is identified by NDC 10742-8397 and is authorized under FDA application M006.

Identification & Billing

NDC Package Code
10742-8397-2
Package Description
185 mL in 1 TUBE
Product Code
10742-8397
11-Digit Billing Format
10742839702

Clinical Specifications

Proprietary Name
Oxy Face Wash Maximum Aciton
Dosage Form
-

Regulatory & Marketing

Labeler Name
The Mentholatum Company
FDA Application #
M006
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-01-2016
End Marketing Date
06-30-2025
Listing Expiration
06-30-2025
Exclude Flag
D
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (10742-8397). Click a package code to view its specific billing and regulatory data.

10742-8397-1
147.7 mL in 1 TUBE

* 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 10742-8397-2 identifies a specific commercial package of 185 ml in 1 tube of Oxy Face Wash Maximum Aciton, labeled by The Mentholatum Company. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by The Mentholatum Company on August 01, 2016. The current certification is valid through June 30, 2025.

How is this The Mentholatum Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10742839702. 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 (5-4-1)
10742-8397-2
11-Digit CMS (5-4-2)
10742-8397-02

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