Cold And Flu Kit
NDC Package 0363-6406-22
Package Information
Cold And Flu (acetaminophen, dextromethorphan hbr, doxylamine succinate, guaifenesin, phenylephrine hcl) kits is do not take more than directeddo not take more than 8 caplets of Daytime and Nighttime products in any 24-hour periodadults and children 12 years and over: take 2 caplets with water every 4 hourschildren under 12 years: ask a doctor. This formulation utilizes a kit delivery system. Marketed by Walgreen Company, this product is identified by NDC 0363-6406 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0363 - Walgreen Company
- 0363-6406 - Cold And Flu
- 0363-6406-22 - 1 KIT in 1 PACKAGE, COMBINATION * 8 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK
- 0363-6406 - Cold And Flu
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 (0363-6406). 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 0363-6406-22 identifies a specific commercial package of 1 kit in 1 package, combination * 8 tablet, film coated in 1 blister pack * 8 tablet, film coated in 1 blister pack of Cold And Flu Daytime, Nighttime, Maximum Strength, a human over the counter drug labeled by Walgreen Company. This kit is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Walgreen Company on August 01, 2015. The current certification is valid through December 31, 2027.
How is this Walgreen Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363640622. 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 Labeler segment to maintain the 5-4-2 structure.
