Benzoil 12hr Acne Treatment
NDC Package 71792-101-11

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Benzoil 12hr Acne Treatment is sENSITIVITY TEST FOR A NEW USER. Marketed by The Skincare Company, Inc., this product is identified by NDC 71792-101 and is authorized under FDA application M006.

Identification & Billing

NDC Package Code
71792-101-11
Package Description
60 mL in 1 TUBE
Product Code
71792-101
11-Digit Billing Format
71792010111
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Benzoil 12hr Acne Treatment
Dosage Form
-
Usage Information
SENSITIVITY TEST FOR A NEW USER. APPLY PRODUCT SPARINGLY TO ONE OR TWO SMALL AFFECTED AREAS DURING THE FIRST 3 DAYS. IF NO DISCOMFORT OCCURS, FOLLOW THE DIRECTIONS STATED BELOW.CLEAN THE SKIN THOROUGHLY BEFORE APPLYING THIS PRODUCT.COVER THE ENTIRE AFFECTED AREA WITH A THIN LAYER ONE TO THREE TIMES DAILY.BECAUSE EXCESSIVE DRYING OF THE SKIN MAY OCCUR, START WITH ONE APPLICATION DAILY, THEN GRADUALLY INCREASE TO TWO OR THREE TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCTOR.IF BOTHERSOME DRYNESS OR PEELING OCCURS, REDUCE APPLICATION TO ONCE A DAY OR EVERY OTHER DAY.IF GOING OUTSIDE, APPLY SUNSCREEN AFTER USING THIS PRODUCT. IF IRRITATION OR SENSITIVITY DEVELOPS, STOP USE OF BOTH PRODUCTS AND ASK A DOCTOR.

Regulatory & Marketing

Labeler Name
The Skincare Company, Inc.
FDA Application #
M006
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-12-2017
Listing Expiration
12-31-2025
Exclude Flag
I
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 71792-101-11 identifies a specific commercial package of 60 ml in 1 tube of Benzoil 12hr Acne Treatment, labeled by The Skincare Company, Inc.. 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 Skincare Company, Inc. on October 12, 2017. The current certification is valid through December 31, 2025.

How is this The Skincare Company, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71792010111. 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)
71792-101-11
11-Digit CMS (5-4-2)
71792-0101-11

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