Iontophoresis
NDC Package 51985-010-01

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.

Iontophoresis is directions:Apply Anti aging serum and pat gently for about a minute.Peel patch from liner and turn over. Marketed by Rocket Electric Co., Ltd., this product is identified by NDC 51985-010 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
51985-010-01
Package Description
20 mL in 1 CARTON
Product Code
51985-010
11-Digit Billing Format
51985001001

Clinical Specifications

Proprietary Name
Iontophoresis Anti Aging Solution I
Dosage Form
-
Usage Information
Directions:Apply Anti aging serum and pat gently for about a minute.Peel patch from liner and turn over. black side onto skin.Place patch around eye and leave on for 1 hour then remove.

Regulatory & Marketing

Labeler Name
Rocket Electric Co., Ltd.
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-01-2010
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 51985-010-01 identifies a specific commercial package of 20 ml in 1 carton of Iontophoresis Anti Aging Solution I, labeled by Rocket Electric Co., Ltd.. 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 Rocket Electric Co., Ltd. on April 01, 2010. The current certification is valid through December 31, 2017.

How is this Rocket Electric Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51985001001. 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)
51985-010-01
11-Digit CMS (5-4-2)
51985-0010-01

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