NDC Package 79903-053-24 Extra Strength Pain Reliever Pm

Acetaminophen And Diphenhydramine Hydrochloride 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:
79903-053-24
Package Description:
1 BOTTLE in 1 CARTON / 24 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Extra Strength Pain Reliever Pm
Non-Proprietary Name:
Acetaminophen And Diphenhydramine Hydrochloride
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride
Usage Information:
Do not take more than directed(see Overdose warning) adults and children 12 years of age and over:take 2 caplets at bedtime or as directed by a doctordo not take more than 2 caplets in a 24 hour periodchildren under 12 years of age:do not use this adult product in children under 12 years of age. This will provide more than the recommended dose (overdose) and may cause liver damage
11-Digit NDC Billing Format:
79903005324
NDC to 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
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Walmart Inc.
    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.
  • Sample Package:
    No
    FDA Application Number:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-13-2021
    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
    79903-053-10100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 79903-053-24?

    The NDC Packaged Code 79903-053-24 is assigned to a package of 1 bottle in 1 carton / 24 tablet in 1 bottle of Extra Strength Pain Reliever Pm, a human over the counter drug labeled by Walmart Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 79903-053 included in the NDC Directory?

    Yes, Extra Strength Pain Reliever Pm with product code 79903-053 is active and included in the NDC Directory. The product was first marketed by Walmart Inc. on January 13, 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 79903-053-24?

    The 11-digit format is 79903005324. 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
    5-3-279903-053-245-4-279903-0053-24