Right Remedies Mucus Relief Dm Tablet
NDC Package 70692-181-25

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Right Remedies Mucus Relief Dm (dextromethorphan hydrobromide, guaifenesin) tablets is • do not exceed 6 tablets in 24 hours, unless directed by a doctoradults and children 12 years of age and overtake 1 tablet every 4 hours with a full glass of water while symptoms persistc​hildren under 12 years of agedo not use. This formulation utilizes a tablet delivery system. Marketed by Strive Pharmaceuticals Inc., this product is identified by NDC 70692-181 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
70692-181-25
Package Description
250 TABLET in 1 BOTTLE
Product Code
70692-181
11-Digit Billing Format
70692018125

Clinical Specifications

Proprietary Name
Right Remedies Mucus Relief Dm
Non-Proprietary Name
Dextromethorphan Hydrobromide, Guaifenesin
Substance Name
Dextromethorphan Hydrobromide; Guaifenesin
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
• do not exceed 6 tablets in 24 hours, unless directed by a doctoradults and children 12 years of age and overtake 1 tablet every 4 hours with a full glass of water while symptoms persistc​hildren under 12 years of agedo not use

Regulatory & Marketing

Labeler Name
Strive Pharmaceuticals Inc.
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-01-2026
Listing Expiration
12-31-2027
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (70692-181). Click a package code to view its specific billing and regulatory data.

70692-181-81
180 TABLET in 1 BOTTLE

* 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 70692-181-25 identifies a specific commercial package of 250 tablet in 1 bottle of Right Remedies Mucus Relief Dm, a human over the counter drug labeled by Strive Pharmaceuticals Inc.. This tablet is formulated for oral use and contains dextromethorphan hydrobromide; guaifenesin as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Strive Pharmaceuticals Inc. on June 01, 2026. The current certification is valid through December 31, 2027.

How is this Strive Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70692018125. 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)
70692-181-25
11-Digit CMS (5-4-2)
70692-0181-25

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