Medique Medi-mucus Tablet
NDC Package 47682-432-50
Package Information
Medique Medi-mucus (dextromethorphan hbr, guaifenesin) tablets is useshelps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productiveTemporarily relieves:cough due to minor throat irritations as may occur with the common cold or inhaled irritantsthe intensity of coughingthe impulse to cough to help you get sleep. This formulation utilizes a tablet delivery system. Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-432 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1147685 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral Tablet
- RxCUI: 1147685 - dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral Tablet
- RxCUI: 1147685 - guaifenesin 400 MG / dextromethorphan HBr 20 MG Oral Tablet
Clinical Specifications
- Decreased Respiratory Secretion Viscosity - [PE] (Physiologic Effect)
- Expectorant - [EPC] (Established Pharmacologic Class)
- Increased Respiratory Secretions - [PE] (Physiologic Effect)
- Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
- Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
- Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
- Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
Regulatory & Marketing
Hierarchy Structure
- 47682 - Unifirst First Aid Corporation
- 47682-432 - Medique Medi-mucus
- 47682-432-50 - 50 PACKET in 1 BOX / 1 TABLET in 1 PACKET (47682-432-46)
- 47682-432 - Medique Medi-mucus
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 (47682-432). Click a package code to view its specific billing and regulatory data.
* 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 47682-432-50 identifies a specific commercial package of 50 packet in 1 box / 1 tablet in 1 packet (47682-432-46) of Medique Medi-mucus, a human over the counter drug labeled by Unifirst First Aid Corporation. 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 Unifirst First Aid Corporation on May 01, 2023. The current certification is valid through December 31, 2026.
How is this Unifirst First Aid Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 47682043250. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.
