NDC Package 69423-985-02 Vicks Zzzquil Night Pain

Diphenhydramine Hydrochloride And Acetaminophen Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
69423-985-02
Package Description:
2 BOTTLE in 1 CARTON / 354 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Vicks Zzzquil Night Pain
Non-Proprietary Name:
Diphenhydramine Hydrochloride And Acetaminophen
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride
Usage Information:
Take only one dose (30 mL) per day (24 hours)only use the dose cup providedadults & children 12 yrs & over30 mL at bedtimechildren under 12 yrsdo not use
11-Digit NDC Billing Format:
69423098502
NDC to RxNorm Crosswalk:
  • RxCUI: 1092373 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG in 15 mL Oral Solution
  • RxCUI: 1092373 - acetaminophen 33.3 MG/ML / diphenhydramine hydrochloride 1.67 MG/ML Oral Solution
  • RxCUI: 1092373 - acetaminophen 1000 MG / diphenhydramine HCl 50 MG per 30 ML Oral Solution
  • RxCUI: 1092373 - acetaminophen 500 MG / diphenhydramine HCl 25 MG per 15 ML Oral Solution
  • RxCUI: 1092373 - APAP 33.3 MG/ML / Diphenhydramine Hydrochloride 1.67 MG/ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    The Procter & Gamble Manufacturing Company
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M010
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-03-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    69423-985-12354 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69423-985-02?

    The NDC Packaged Code 69423-985-02 is assigned to a package of 2 bottle in 1 carton / 354 ml in 1 bottle of Vicks Zzzquil Night Pain, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is liquid and is administered via oral form.

    Is NDC 69423-985 included in the NDC Directory?

    Yes, Vicks Zzzquil Night Pain with product code 69423-985 is active and included in the NDC Directory. The product was first marketed by The Procter & Gamble Manufacturing Company on March 03, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69423-985-02?

    The 11-digit format is 69423098502. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-269423-985-025-4-269423-0985-02