Dayquil Severe
NDC Package 73097-006-50

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Dayquil Severe is • take only as directed • do not exceed 8 caplets in 24 hrsadults & children 12 years & over 2 caplets with water every 4 hours children 4 to under 12 years ask a doctor children under 4 years do not use. Marketed by Savings Distributors Llc, this product is identified by NDC 73097-006 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
73097-006-50
Package Description
25 POUCH in 1 CARTON / 2 TABLET in 1 POUCH
Product Code
73097-006
11-Digit Billing Format
73097000650
RxNorm Crosswalk
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet

Clinical Specifications

Proprietary Name
Dayquil Severe
Dosage Form
-
Usage Information
• take only as directed • do not exceed 8 caplets in 24 hrsadults & children 12 years & over 2 caplets with water every 4 hours children 4 to under 12 years ask a doctor children under 4 years do not use

Regulatory & Marketing

Labeler Name
Savings Distributors Llc
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-05-2019
Listing Expiration
12-31-2020
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (73097-006). Click a package code to view its specific billing and regulatory data.

73097-006-02
1 POUCH in 1 CARTON / 2 TABLET in 1 POUCH
73097-006-40
20 POUCH in 1 CARTON / 2 TABLET in 1 POUCH

* 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 73097-006-50 identifies a specific commercial package of 25 pouch in 1 carton / 2 tablet in 1 pouch of Dayquil Severe, labeled by Savings Distributors Llc. 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 Savings Distributors Llc on July 05, 2019. The current certification is valid through December 31, 2020.

How is this Savings Distributors Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73097000650. 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)
73097-006-50
11-Digit CMS (5-4-2)
73097-0006-50

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