Careone Daytime Severe Cold And Cough
NDC Package 41520-330-06

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.

Careone Daytime Severe Cold And Cough is when using this product - do not exceed recommended dosage. Marketed by American Sales Company, this product is identified by NDC 41520-330 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
41520-330-06
Package Description
6 GRANULE, FOR SOLUTION in 1 BOX
Product Code
41520-330
11-Digit Billing Format
41520033006
RxNorm Crosswalk
  • RxCUI: 1659967 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Granules for Oral Solution
  • RxCUI: 1659967 - acetaminophen 650 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
  • RxCUI: 1659967 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Powder for Oral Solution
  • RxCUI: 1659967 - APAP 650 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Granules for Oral Solution

Clinical Specifications

Proprietary Name
Careone Daytime Severe Cold And Cough Berry Infused With Menthol And Green Tea Flavors
Dosage Form
-
Usage Information
When using this product - do not exceed recommended dosage.

Regulatory & Marketing

Labeler Name
American Sales Company
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-31-2013
Listing Expiration
12-31-2019
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 41520-330-06 identifies a specific commercial package of 6 granule, for solution in 1 box of Careone Daytime Severe Cold And Cough Berry Infused With Menthol And Green Tea Flavors, labeled by American Sales 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 American Sales Company on July 31, 2013. The current certification is valid through December 31, 2019.

How is this American Sales Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41520033006. 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)
41520-330-06
11-Digit CMS (5-4-2)
41520-0330-06

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