Vicks Sinex D
NDC Package 37000-921-30

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

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

Vicks Sinex D is a . Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 37000-921 and is authorized under FDA application ANDA076518.

Identification & Billing

NDC Package Code
37000-921-30
Package Description
3 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Code
37000-921
11-Digit Billing Format
37000092130

Clinical Specifications

Proprietary Name
Vicks Sinex D Severe Sinus And Cold
Dosage Form
-

Regulatory & Marketing

Labeler Name
The Procter & Gamble Manufacturing Company
FDA Application #
ANDA076518
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
12-17-2018
End Marketing Date
03-01-2021
Listing Expiration
03-01-2021
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 37000-921-30 identifies a specific commercial package of 3 blister pack in 1 carton / 10 tablet in 1 blister pack of Vicks Sinex D Severe Sinus And Cold, labeled by The 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 The Procter & Gamble Manufacturing Company on December 17, 2018. The current certification is valid through March 01, 2021.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37000092130. 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)
37000-921-30
11-Digit CMS (5-4-2)
37000-0921-30

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