Medi Hydro Dp B Tox Ampoule
NDC Package 70694-0010-1

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.

Medi Hydro Dp B Tox Ampoule is open the lid, press the lid to fill the dropper and apply evenly 3-4 drops to the desired parts, gently tap with the fingers to allow it to absorb. Marketed by Inc Mbg, this product is identified by NDC 70694-0010.

Identification & Billing

NDC Package Code
70694-0010-1
Package Description
30 mL in 1 BOTTLE
Product Code
70694-0010
11-Digit Billing Format
70694001001

Clinical Specifications

Proprietary Name
Medi Hydro Dp B Tox Ampoule
Dosage Form
-
Usage Information
Open the lid, press the lid to fill the dropper and apply evenly 3-4 drops to the desired parts, gently tap with the fingers to allow it to absorb

Regulatory & Marketing

Labeler Name
Inc Mbg
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
01-24-2019
Listing Expiration
12-31-2020
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 70694-0010-1 identifies a specific commercial package of 30 ml in 1 bottle of Medi Hydro Dp B Tox Ampoule, labeled by Inc Mbg. 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 Inc Mbg on January 24, 2019. The current certification is valid through December 31, 2020.

How is this Inc Mbg product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70694001001. 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)
70694-0010-1
11-Digit CMS (5-4-2)
70694-0010-01

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