Vicks Zzzquil Tablet, Coated
NDC Package 37000-974-60

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

Package Information

Vicks Zzzquil (diphenhydramine hydrochloride and acetaminophen) tablets is take only 2 geltabs per day (24 hours)adults & children 12 yrs & over2 gletabs at bedtimechildren under 12 yrsdo not use. This formulation utilizes a tablet, coated delivery system. Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 37000-974 and is authorized under FDA application M010.

Identification & Billing

NDC Package Code
37000-974-60
Package Description
1 BOTTLE in 1 CARTON / 60 TABLET, COATED in 1 BOTTLE
Product Code
37000-974
11-Digit Billing Format
37000097460
RxNorm Crosswalk
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1092189 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet

Clinical Specifications

Proprietary Name
Vicks Zzzquil Night Pain
Non-Proprietary Name
Diphenhydramine Hydrochloride And Acetaminophen
Substance Name
Acetaminophen; Diphenhydramine Hydrochloride
Dosage Form
Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Take only 2 geltabs per day (24 hours)adults & children 12 yrs & over2 gletabs at bedtimechildren under 12 yrsdo not use

Regulatory & Marketing

Labeler Name
The Procter & Gamble Manufacturing Company
Product Type
Human Otc Drug
FDA Application #
M010
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-01-2020
Listing Expiration
12-31-2027
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 37000-974-60 identifies a specific commercial package of 1 bottle in 1 carton / 60 tablet, coated in 1 bottle of Vicks Zzzquil Night Pain, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. This tablet, coated is formulated for oral use and contains acetaminophen; diphenhydramine 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 The Procter & Gamble Manufacturing Company on June 01, 2020. The current certification is valid through December 31, 2027.

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: 37000097460. 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)
37000-974-60
11-Digit CMS (5-4-2)
37000-0974-60

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