Gout Reliever Synergy
NDC Package 70470-1113-5

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.

Gout Reliever Synergy is dosage and UsageAdults 5ml maximum per dayApply on skin and gentle massage around painful area. Marketed by Phytopia Co., Ltd., this product is identified by NDC 70470-1113 and is authorized under FDA application part346.

Identification & Billing

NDC Package Code
70470-1113-5
Package Description
500 mg in 1 BOTTLE, GLASS
Product Code
70470-1113
11-Digit Billing Format
70470111305

Clinical Specifications

Proprietary Name
Gout Reliever Synergy
Dosage Form
-
Usage Information
Dosage and UsageAdults 5ml maximum per dayApply on skin and gentle massage around painful area.

Regulatory & Marketing

Labeler Name
Phytopia Co., Ltd.
FDA Application #
part346
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-01-2016
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 70470-1113-5 identifies a specific commercial package of 500 mg in 1 bottle, glass of Gout Reliever Synergy, labeled by Phytopia 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 Phytopia Co., Ltd. on April 01, 2016. The current certification is valid through December 31, 2017.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70470111305. 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)
70470-1113-5
11-Digit CMS (5-4-2)
70470-1113-05

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