Children Acetaminophen Oral Solution
NDC Package 17856-7014-9
Package Information
Children Acetaminophen Oral Solution is Usestemporarily relieves minor aches and pains due to:headachemuscular achesbackacheminor pain of arthritisthe common coldtoothachepremenstrual and menstrual crampstemporarily reduces fever. Marketed by Atlantic Biologicals Corp., this product is identified by NDC 17856-7014 and is authorized under FDA application M.
Identification & Billing
- RxCUI: 307675 - acetaminophen 160 MG in 5 mL Oral Solution
- RxCUI: 307675 - acetaminophen 32 MG/ML Oral Solution
- RxCUI: 307675 - acetaminophen 160 MG per 5 ML Oral Solution
- RxCUI: 307675 - acetaminophen 325 MG per 10.15 ML Oral Solution
- RxCUI: 307675 - acetaminophen 650 MG per 20.3 ML Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 17856 - Atlantic Biologicals Corp.
- 17856-7014 - Children Acetaminophen Oral Solution
- 17856-7014-9 - 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 10.15 mL in 1 CUP, UNIT-DOSE
- 17856-7014 - Children Acetaminophen Oral Solution
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (17856-7014). Click a package code to view its specific billing and regulatory data.
* 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 17856-7014-9 identifies a specific commercial package of 72 cup, unit-dose in 1 box, unit-dose / 10.15 ml in 1 cup, unit-dose of Children Acetaminophen Oral Solution, labeled by Atlantic Biologicals Corp.. 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 Atlantic Biologicals Corp. on October 01, 2019. The current certification is valid through December 31, 2025.
How is this Atlantic Biologicals Corp. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 17856701409. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.
