Acetaminophen (red)
NDC Package 55629-718-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Acetaminophen (red) is do not take more than directed(seeOverdose warning) adults and children 12 years and overtake 2 softgels every 4 to 6 hours while symptoms lastdo not take more than 10 softgels in 24 hoursdo not use for more than 10 days unless directed by a doctor children 6-11 yearstake 1 softgel every 4 to 6 hours while symptoms lastdo not take more than 5 softgels in 24 hoursdo not use for more than 5 days unless directed by a doctor children under 6 years ask a doctor. Marketed by One2zee Limited Liability Company, this product is identified by NDC 55629-718 and is authorized under FDA application part343.

Identification & Billing

NDC Package Code
55629-718-01
Package Description
48 BAG in 1 BOX / 300 CAPSULE, LIQUID FILLED in 1 BAG (55629-718-02)
Product Code
11-Digit Billing Format
55629071801
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Acetaminophen (red)
Dosage Form
-
Usage Information
Do not take more than directed(seeOverdose warning) adults and children 12 years and overtake 2 softgels every 4 to 6 hours while symptoms lastdo not take more than 10 softgels in 24 hoursdo not use for more than 10 days unless directed by a doctor children 6-11 yearstake 1 softgel every 4 to 6 hours while symptoms lastdo not take more than 5 softgels in 24 hoursdo not use for more than 5 days unless directed by a doctor children under 6 years ask a doctor

Regulatory & Marketing

Labeler Name
One2zee Limited Liability Company
FDA Application #
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
02-25-2019
Listing Expiration
12-31-2020
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 55629-718-01 identifies a specific commercial package of 48 bag in 1 box / 300 capsule, liquid filled in 1 bag (55629-718-02) of Acetaminophen (red), labeled by One2zee Limited Liability Company. 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 One2zee Limited Liability Company on February 25, 2019. The current certification is valid through December 31, 2020.

How is this One2zee Limited Liability Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55629071801. 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)
55629-718-01
11-Digit CMS (5-4-2)
55629-0718-01

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