Dual Action Tablet, Film Coated
NDC Package 72288-542-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Dual Action (acetaminophen, ibuprofen) tablets is •do not take more than directed adults and children 12 years and over•take 2 caplets every 8  hours while symptoms persist children under 12 years•ask a doctor•do not take more than 6 caplets in 24 hours, unless directed by a doctor. This formulation utilizes a tablet, film coated delivery system. Marketed by Amazon.com Services Llc, this product is identified by NDC 72288-542 and is authorized under FDA application ANDA214836.

Identification & Billing

NDC Package Code
72288-542-01
Package Description
1 BOTTLE in 1 CARTON / 216 TABLET, FILM COATED in 1 BOTTLE (72288-542-00)
Product Code
72288-542
11-Digit Billing Format
72288054201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Dual Action
Non-Proprietary Name
Acetaminophen, Ibuprofen
Substance Name
Acetaminophen; Ibuprofen
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
•do not take more than directed adults and children 12 years and over•take 2 caplets every 8  hours while symptoms persist children under 12 years•ask a doctor•do not take more than 6 caplets in 24 hours, unless directed by a doctor

Regulatory & Marketing

Labeler Name
Amazon.com Services Llc
Product Type
Human Otc Drug
FDA Application #
ANDA214836
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
05-18-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 72288-542-01 identifies a specific commercial package of 1 bottle in 1 carton / 216 tablet, film coated in 1 bottle (72288-542-00) of Dual Action, a human over the counter drug labeled by Amazon.com Services Llc. This tablet, film coated is formulated for oral use and contains acetaminophen; ibuprofen as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Amazon.com Services Llc on May 18, 2026. The current certification is valid through December 31, 2027.

How is this Amazon.com Services Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72288054201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
72288-542-01
11-Digit CMS (5-4-2)
72288-0542-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.