NDC Package 70692-142-31 Headache Relief

Acetaminophen,Aspirin,Caffeine Tablet, 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:
70692-142-31
Package Description:
300 TABLET, COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Headache Relief
Non-Proprietary Name:
Acetaminophen, Aspirin, Caffeine
Substance Name:
Acetaminophen; Aspirin; Caffeine
Usage Information:
• do not use more than directed (see overdose warning)• drink a full glass of water with each dose• adults and children 12 years and over: take 2 caplets every 6 hours; not more than 8 caplets in 24 hours• children under 12 years: ask a doctor
11-Digit NDC Billing Format:
70692014231
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:
    Strive Pharmaceuticals Inc.
    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(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    part343
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    04-06-2023
    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.

    Frequently Asked Questions

    What is NDC 70692-142-31?

    The NDC Packaged Code 70692-142-31 is assigned to a package of 300 tablet, coated in 1 bottle of Headache Relief, a human over the counter drug labeled by Strive Pharmaceuticals Inc.. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 70692-142 included in the NDC Directory?

    Yes, Headache Relief with product code 70692-142 is active and included in the NDC Directory. The product was first marketed by Strive Pharmaceuticals Inc. on April 06, 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 70692-142-31?

    The 11-digit format is 70692014231. 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
    5-3-270692-142-315-4-270692-0142-31