Severe Cold And Cough Daytime
NDC Package 63868-290-06

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.

Severe Cold And Cough Daytime is •do not use more than directed•take every 4 hours; while symptoms persist. Marketed by Chain Drug Manufacturing Assn, this product is identified by NDC 63868-290 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
63868-290-06
Package Description
6 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET
Product Code
63868-290
11-Digit Billing Format
63868029006
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
Severe Cold And Cough Daytime
Dosage Form
-
Usage Information
•do not use more than directed•take every 4 hours; while symptoms persist. Do not to exceed 5 packets in 24 hours unless directed by a doctorAgeDoseAdults and children 12 years of age and overOne packetChildren under 12 years of ageDo not use•dissolve contents of one packet into 8 oz hot water; sip while hot. Consume entire drink within 10-15 minutes•If using a microwave, add contents of one packet 8 oz. of cool water: Stir briskly before and after heating: Do not overheat.

Regulatory & Marketing

Labeler Name
Chain Drug Manufacturing Assn
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-25-2018
Listing Expiration
12-31-2023
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 63868-290-06 identifies a specific commercial package of 6 packet in 1 carton / 1 powder, for solution in 1 packet of Severe Cold And Cough Daytime, labeled by Chain Drug Manufacturing Assn. 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 Chain Drug Manufacturing Assn on July 25, 2018. The current certification is valid through December 31, 2023.

How is this Chain Drug Manufacturing Assn product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63868029006. 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)
63868-290-06
11-Digit CMS (5-4-2)
63868-0290-06

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