Extra Strenghth Acetaminophen
NDC Package 69729-107-40

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Extra Strenghth Acetaminophen is  do not use more than directed (see overdose warning)Adults and children 12 years of age and older: Take 2 caplets every 6 hours while symptoms last. Marketed by Opmx Llc, this product is identified by NDC 69729-107 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
69729-107-40
Package Description
1 BOTTLE in 1 CARTON / 40 TABLET in 1 BOTTLE
Product Code
69729-107
11-Digit Billing Format
69729010740
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Extra Strenghth Acetaminophen
Dosage Form
-
Usage Information
 do not use more than directed (see overdose warning)Adults and children 12 years of age and older: Take 2 caplets every 6 hours while symptoms last. Do not take more than 6 caplets in 24 hours, unless directed by a doctorDo not use more than 10 days unless directed by a doctor.Children under 12 years of age: Do not use this extra strength product. This will provide more than the recommended dose (overdose) and could cause serious health problems.

Regulatory & Marketing

Labeler Name
Opmx Llc
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-31-2017
Listing Expiration
12-31-2026
Exclude Flag
I
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 69729-107-40 identifies a specific commercial package of 1 bottle in 1 carton / 40 tablet in 1 bottle of Extra Strenghth Acetaminophen, labeled by Opmx Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Opmx Llc on July 31, 2017. The current certification is valid through December 31, 2026.

How is this Opmx Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69729010740. 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)
69729-107-40
11-Digit CMS (5-4-2)
69729-0107-40

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