Vicks Dayquil Hot Remedy Rapid Relief Multi-symptom Powder, For Solution
NDC Package 58933-550-08

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

Vicks Dayquil Hot Remedy Rapid Relief Multi-symptom (acetaminophen, dextromethorphan hbr, phenylephrine hcl) powders is • take only as directed• do not exceed 6 doses per 24 hrs• Dissolve contents of one packet into 8 oz. This formulation utilizes a powder, for solution delivery system. Marketed by Procter & Gamble Manufactura S De Rl De Cv, this product is identified by NDC 58933-550 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
58933-550-08
Package Description
8 PACKET in 1 PACKAGE / 5 g in 1 PACKET
Product Code
58933-550
11-Digit Billing Format
58933055008
RxNorm Crosswalk
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Granules for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Packet for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Powder for Oral Solution
  • RxCUI: 1189316 - APAP 500 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Granules for Oral Solution

Clinical Specifications

Proprietary Name
Vicks Dayquil Hot Remedy Rapid Relief Multi-symptom Cold And Flu Plus Congestion
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Dosage Form
Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
• take only as directed• do not exceed 6 doses per 24 hrs• Dissolve contents of one packet into 8 oz. of hot water and stir briskly; sip while hot. Consume entire drink within 10-15 minutes• If using a microwave, add contents of one packet to 8 oz. of cool water, stir briskly before and after heating. Do not overheatAdults & children 12 yrs & over - one packet (dose) every 4 hoursChildren under 12 yrs - Do not use • take only as directed• do not exceed 6 doses per 24 hrs• Dissolve contents of one packet into 8 oz. of hot water and stir briskly; sip while hot. Consume entire drink within 10-15 minutes• If using a microwave, add contents of one packet to 8 oz. of cool water, stir briskly before and after heating. Do not overheatAdults & children 12 yrs & over - one packet (dose) every 4 hoursChildren under 12 yrs - Do not use

Regulatory & Marketing

Labeler Name
Procter & Gamble Manufactura S De Rl De Cv
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-22-2023
End Marketing Date
06-30-2027
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 (58933-550). Click a package code to view its specific billing and regulatory data.

58933-550-01
5 g in 1 PACKET

* 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 58933-550-08 identifies a specific commercial package of 8 packet in 1 package / 5 g in 1 packet of Vicks Dayquil Hot Remedy Rapid Relief Multi-symptom Cold And Flu Plus Congestion, a human over the counter drug labeled by Procter & Gamble Manufactura S De Rl De Cv. This powder, for solution is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; 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 Procter & Gamble Manufactura S De Rl De Cv on March 22, 2023.

How is this Procter & Gamble Manufactura S De Rl De Cv product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 58933055008. 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)
58933-550-08
11-Digit CMS (5-4-2)
58933-0550-08

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