Daytime Cold And Flu
NDC Package 62011-0318-1

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 Cold And Flu is a medication used as Pain relieverCough SuppressantNasal decongestant. Marketed by Mckesson, this product is identified by NDC 62011-0318 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
62011-0318-1
Package Description
24 CARTON in 1 BLISTER PACK / 1 CAPSULE, LIQUID FILLED in 1 CARTON
Product Code
62011-0318
11-Digit Billing Format
62011031801
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
24 EA
RxNorm Crosswalk
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule

Clinical Specifications

Proprietary Name
Daytime Cold And Flu
Dosage Form
-
Usage Information
This product is used as Pain relieverCough SuppressantNasal decongestant. Pain reliever, cough suppressant and Nasal decongestant

Regulatory & Marketing

Labeler Name
Mckesson
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
11-25-2016
Listing Expiration
12-31-2017
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 62011-0318-1 identifies a specific commercial package of 24 carton in 1 blister pack / 1 capsule, liquid filled in 1 carton of Daytime Cold And Flu, labeled by Mckesson. This product is billed for "EA" each discreet unit and contains an estimated amount of 24 billable units per package. 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 Mckesson on November 25, 2016. The current certification is valid through December 31, 2017.

How is this Mckesson product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62011031801. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 24 total billable units per package. 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 (5-4-1)
62011-0318-1
11-Digit CMS (5-4-2)
62011-0318-01

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