Multi-symptom Cold Relief Tablet, Film Coated
NDC Package 47682-047-99

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

Multi-symptom Cold Relief (acetaminophen, dextromethorphan hbr, phenylephrine hcl , guaifenesin, ,) tablets is usesTemporarily relieves these symptoms due to the common coldheadachenasal congestioncoughminor aches and painssore throatsinus congestion and pressurehelps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make cough more productiveTemporarily reduces fever. This formulation utilizes a tablet, film coated delivery system. Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-047 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
47682-047-99
Package Description
2 TABLET, FILM COATED in 1 PACKET
Product Code
47682-047
11-Digit Billing Format
47682004799
RxNorm Crosswalk
  • RxCUI: 1098435 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 100 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1098435 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1098435 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / Guaifenesin 100 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet

Clinical Specifications

Proprietary Name
Multi-symptom Cold Relief
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl , Guaifenesin, ,
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Dosage Form
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
UsesTemporarily relieves these symptoms due to the common coldheadachenasal congestioncoughminor aches and painssore throatsinus congestion and pressurehelps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make cough more productiveTemporarily reduces fever.

Regulatory & Marketing

Labeler Name
Unifirst First Aid Corporation
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-26-2022
Listing Expiration
12-31-2026
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 (47682-047). Click a package code to view its specific billing and regulatory data.

47682-047-47
100 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET (47682-047-99)
47682-047-80
40 PACKET in 1 BOX / 2 TABLET, FILM COATED in 1 PACKET (47682-047-99)

* 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 47682-047-99 identifies a specific commercial package of 2 tablet, film coated in 1 packet of Multi-symptom Cold Relief, a human over the counter drug labeled by Unifirst First Aid Corporation. This tablet, film coated is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; guaifenesin; phenylephrine hydrochloride 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 September 26, 2022. 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: 47682004799. 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)
47682-047-99
11-Digit CMS (5-4-2)
47682-0047-99

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