Rg Td5 Inv.solid Antiperspirant Deodorant Fresh Blast
NDC Package 54340-751-01

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.

Rg Td5 Inv.solid Antiperspirant Deodorant Fresh Blast is use:  Reduces underarm perspiration , Extra effective. Marketed by The Dial Corporation, this product is identified by NDC 54340-751 and is authorized under FDA application part350.

Identification & Billing

NDC Package Code
54340-751-01
Package Description
11.9 g in 1 CANISTER
Product Code
54340-751
11-Digit Billing Format
54340075101

Clinical Specifications

Proprietary Name
Rg Td5 Inv.solid Antiperspirant Deodorant Fresh Blast
Dosage Form
-
Usage Information
Use:  Reduces underarm perspiration , Extra effective

Regulatory & Marketing

Labeler Name
The Dial Corporation
FDA Application #
part350
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
10-27-2011
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 54340-751-01 identifies a specific commercial package of 11.9 g in 1 canister of Rg Td5 Inv.solid Antiperspirant Deodorant Fresh Blast, 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 October 27, 2011. 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: 54340075101. 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)
54340-751-01
11-Digit CMS (5-4-2)
54340-0751-01

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