Vicks Nyquil
NDC Package 37000-554-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Vicks Nyquil is a . Marketed by Procter & Gamble Manufacturing Company, this product is identified by NDC 37000-554 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
37000-554-10
Package Description
295 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
37000055410

Clinical Specifications

Proprietary Name
Vicks Nyquil Cold And Flu Nighttime Relief
Dosage Form
-

Regulatory & Marketing

Labeler Name
Procter & Gamble Manufacturing Company
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-20-2009
End Marketing Date
06-01-2010
Listing Expiration
06-01-2010
Exclude Flag
D
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 (37000-554). Click a package code to view its specific billing and regulatory data.

177 mL in 1 BOTTLE, PLASTIC
354 mL in 1 BOTTLE, PLASTIC

* 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 37000-554-10 identifies a specific commercial package of 295 ml in 1 bottle, plastic of Vicks Nyquil Cold And Flu Nighttime Relief, labeled by Procter & Gamble Manufacturing Company. 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 Procter & Gamble Manufacturing Company on April 20, 2009. The current certification is valid through June 01, 2010.

How is this Procter & Gamble Manufacturing Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37000055410. 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)
37000-554-10
11-Digit CMS (5-4-2)
37000-0554-10

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