Elp Essential Dm
NDC Package 70242-139-06

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.

Elp Essential Dm is • Do not take more than 6 doses in any 24-hour period. Marketed by Dannso Corp./d.b.a. Essential Products, this product is identified by NDC 70242-139 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
70242-139-06
Package Description
1 BOTTLE, PLASTIC in 1 BOX / 177 mL in 1 BOTTLE, PLASTIC
Product Code
70242-139
11-Digit Billing Format
70242013906
RxNorm Crosswalk
  • RxCUI: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral Solution

Clinical Specifications

Proprietary Name
Elp Essential Dm
Dosage Form
-
Usage Information
• Do not take more than 6 doses in any 24-hour period. • Shake well before use.Age Dose  Adults and Children 12 years and over 10ml (2 tsps) every 4 hours Children 6 to under 12 years of age. 5ml (1 tsps) every 4 hoursChildren under 6 years of age    Do not use

Regulatory & Marketing

Labeler Name
Dannso Corp./d.b.a. Essential Products
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-26-2023
Listing Expiration
12-31-2024
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 70242-139-06 identifies a specific commercial package of 1 bottle, plastic in 1 box / 177 ml in 1 bottle, plastic of Elp Essential Dm, labeled by Dannso Corp./d.b.a. Essential Products. 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 Dannso Corp./d.b.a. Essential Products on October 26, 2023. The current certification is valid through December 31, 2024.

How is this Dannso Corp./d.b.a. Essential Products product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70242013906. 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)
70242-139-06
11-Digit CMS (5-4-2)
70242-0139-06

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