NDC Package 69423-902-01 Vicks Zzzquil Ultra

Doxylamine Succinate Tablet 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:
69423-902-01
Package Description:
1 TABLET in 1 POUCH
Product Code:
Proprietary Name:
Vicks Zzzquil Ultra
Non-Proprietary Name:
Doxylamine Succinate
Substance Name:
Doxylamine Succinate
Usage Information:
Adults & children 12 yrs & over: take one tablet 30 minutes before going to bed; take once daily or as directed by a doctorchildren under 12 yrs of age: do not use
11-Digit NDC Billing Format:
69423090201
NDC to RxNorm Crosswalk:
  • RxCUI: 1101446 - doxylamine succinate 25 MG Oral Tablet
  • RxCUI: 2548540 - Zzzquil Ultra 25 MG Oral Tablet
  • RxCUI: 2548540 - doxylamine succinate 25 MG Oral Tablet [Zzzquil Ultra]
  • Product Type:
    Human Otc Drug
    Labeler Name:
    The Procter & Gamble Manufacturing Company
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA040167
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-01-2021
    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
    69423-902-121 BLISTER PACK in 1 CARTON / 12 TABLET in 1 BLISTER PACK
    69423-902-242 BLISTER PACK in 1 CARTON / 12 TABLET in 1 BLISTER PACK
    69423-902-3232 POUCH in 1 CARTON / 1 TABLET in 1 POUCH
    69423-902-484 BLISTER PACK in 1 CARTON / 12 TABLET in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69423-902-01?

    The NDC Packaged Code 69423-902-01 is assigned to a package of 1 tablet in 1 pouch of Vicks Zzzquil Ultra, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is tablet and is administered via oral form.

    Is NDC 69423-902 included in the NDC Directory?

    Yes, Vicks Zzzquil Ultra with product code 69423-902 is active and included in the NDC Directory. The product was first marketed by The Procter & Gamble Manufacturing Company on March 01, 2021 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 69423-902-01?

    The 11-digit format is 69423090201. 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
    5-3-269423-902-015-4-269423-0902-01