NDC Package 56062-934-12 Headache Relief

Acetaminophen,Aspirin,Caffeine Tablet, Film Coated 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:
56062-934-12
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Headache Relief
Non-Proprietary Name:
Acetaminophen, Aspirin, Caffeine
Substance Name:
Acetaminophen; Aspirin; Caffeine
Usage Information:
Do not take more than directeddrink a full glass of water with each doseadults and children 12 years and over: take 2 caplets every 6 hours. Do not take more than 8 caplets in 24 hours.children under 12 years: ask a doctor
11-Digit NDC Billing Format:
56062093412
NDC to RxNorm Crosswalk:
  • RxCUI: 308297 - acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet
  • RxCUI: 308297 - APAP 250 MG / ASA 250 MG / caffeine 65 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Publix Super Markets Inc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    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:
    09-24-2021
    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.

    Frequently Asked Questions

    What is NDC 56062-934-12?

    The NDC Packaged Code 56062-934-12 is assigned to a package of 1 bottle, plastic in 1 carton / 100 tablet, film coated in 1 bottle, plastic of Headache Relief, a human over the counter drug labeled by Publix Super Markets Inc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 56062-934 included in the NDC Directory?

    Yes, Headache Relief with product code 56062-934 is active and included in the NDC Directory. The product was first marketed by Publix Super Markets Inc on September 24, 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 56062-934-12?

    The 11-digit format is 56062093412. 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
    5-3-256062-934-125-4-256062-0934-12