Medicated Acne Pads
NDC Package 50730-7701-0

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.

Medicated Acne Pads is cleanse the skin thoroughly before applying medicationUse the pad to wipe the entire affected area and discardDo not leave pad on skin for an extended period of timeRepeat with a clean pad as necessary to remove remaining traces of dirtBecause 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 doctorIf bothersome dryness of peeling occurs, reduce application to once a day or every other day. Marketed by H And P Industries, Inc. Dba Triad Group, this product is identified by NDC 50730-7701 and is authorized under FDA application part333D.

Identification & Billing

NDC Package Code
50730-7701-0
Package Description
1 JAR in 1 BOX / 55 SWAB in 1 JAR
Product Code
50730-7701
11-Digit Billing Format
50730770100
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Medicated Acne Pads
Dosage Form
-
Usage Information
Cleanse the skin thoroughly before applying medicationUse the pad to wipe the entire affected area and discardDo not leave pad on skin for an extended period of timeRepeat with a clean pad as necessary to remove remaining traces of dirtBecause 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 doctorIf bothersome dryness of peeling occurs, reduce application to once a day or every other day

Regulatory & Marketing

Labeler Name
H And P Industries, Inc. Dba Triad Group
FDA Application #
part333D
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
12-02-2003
Listing Expiration
12-31-2017
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 50730-7701-0 identifies a specific commercial package of 1 jar in 1 box / 55 swab in 1 jar of Medicated Acne Pads, labeled by H And P Industries, Inc. Dba Triad Group. 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 H And P Industries, Inc. Dba Triad Group on December 02, 2003. The current certification is valid through December 31, 2017.

How is this H And P Industries, Inc. Dba Triad Group product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50730770100. 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)
50730-7701-0
11-Digit CMS (5-4-2)
50730-7701-00

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