Dial Acne Control Deep Cleansing Body Wash
NDC Package 54340-410-01

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.

Dial Acne Control Deep Cleansing Body Wash is use daily in shower or bath. Marketed by The Dial Corporation, this product is identified by NDC 54340-410 and is authorized under FDA application part358H.

Identification & Billing

NDC Package Code
54340-410-01
Package Description
354 mL in 1 BOTTLE
Product Code
54340-410
11-Digit Billing Format
54340041001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Dial Acne Control Deep Cleansing Body Wash
Dosage Form
-
Usage Information
Use daily in shower or bath. For maximum lather, massage over wet skin with a wash cloth or body poof, concentrating on areas prone to breakouts. Rinse well.

Regulatory & Marketing

Labeler Name
The Dial Corporation
FDA Application #
part358H
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-01-2014
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 54340-410-01 identifies a specific commercial package of 354 ml in 1 bottle of Dial Acne Control Deep Cleansing Body Wash, labeled by The Dial Corporation. 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 Dial Corporation on July 01, 2014. The current certification is valid through December 31, 2017.

How is this The Dial Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54340041001. 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)
54340-410-01
11-Digit CMS (5-4-2)
54340-0410-01

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