Daytime Cough
NDC Package 71027-040-06

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.

Daytime Cough is usesTemporarily relieves these common cold/flu symptoms Minor aches and painsHeadacheSore throatNasal congestionFeverCough due to minor throat and bronchial irritation. Marketed by Kingston Pharma Llc, this product is identified by NDC 71027-040 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
71027-040-06
Package Description
1 BOTTLE in 1 CARTON / 177 mL in 1 BOTTLE
Product Code
71027-040
11-Digit Billing Format
71027004006
RxNorm Crosswalk
  • RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG in 15 mL Oral Solution
  • RxCUI: 1113705 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
  • RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG per 15 ML Oral Solution
  • RxCUI: 1113705 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG per 30 ML Oral Solution
  • RxCUI: 1113705 - APAP 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Daytime Cough
Dosage Form
-
Usage Information
UsesTemporarily relieves these common cold/flu symptoms Minor aches and painsHeadacheSore throatNasal congestionFeverCough due to minor throat and bronchial irritation

Regulatory & Marketing

Labeler Name
Kingston Pharma Llc
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
03-01-2017
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 71027-040-06 identifies a specific commercial package of 1 bottle in 1 carton / 177 ml in 1 bottle of Daytime Cough, labeled by Kingston Pharma 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 Kingston Pharma Llc on March 01, 2017. The current certification is valid through December 31, 2020.

How is this Kingston Pharma Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71027004006. 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)
71027-040-06
11-Digit CMS (5-4-2)
71027-0040-06

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