Cold And Flu Solution
NDC Package 0363-9913-99

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Cold And Flu (acetaminophen, dextromethorphan hbr, doxylamine succinate) solution is do not take more than directedmL = milliliter; FL OZ = fluid ounceonly use the dose cup provideddo not take more than 5 doses per 24 hoursadults and children 12 years and over30 mL every 4 hourschildren 6 to under 12 years15 mL every 4 hourschildren under 6 yearsdo not use do not take more than directeddo not exceed 4 doses per 24 hoursmL = milliliter; FL OZ = fluid ounceonly use the dose cup providedadults and children 12 years and over: 30 mL every 6 hourschildren under 12 years: do not use. This formulation utilizes a solution delivery system. Marketed by Walgreen Company, this product is identified by NDC 0363-9913 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
0363-9913-99
Package Description
2 BOTTLE, PLASTIC in 1 CARTON / 355 mL in 1 BOTTLE, PLASTIC (0363-9913-02)
Product Code
11-Digit Billing Format
00363991399
RxNorm Crosswalk
  • RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 30 mL Oral Solution
  • RxCUI: 1043400 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution
  • RxCUI: 1043400 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG per 15 ML Oral Solution
  • RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG per 30 ML Oral Solution
  • RxCUI: 1043400 - APAP 21.7 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Cold And Flu Night
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Doxylamine Succinate
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
Do not take more than directedmL = milliliter; FL OZ = fluid ounceonly use the dose cup provideddo not take more than 5 doses per 24 hoursadults and children 12 years and over30 mL every 4 hourschildren 6 to under 12 years15 mL every 4 hourschildren under 6 yearsdo not use do not take more than directeddo not exceed 4 doses per 24 hoursmL = milliliter; FL OZ = fluid ounceonly use the dose cup providedadults and children 12 years and over: 30 mL every 6 hourschildren under 12 years: do not use

Regulatory & Marketing

Labeler Name
Walgreen Company
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-14-2022
Listing Expiration
12-31-2026
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0363-9913). Click a package code to view its specific billing and regulatory data.

355 mL in 1 BOTTLE, PLASTIC
2 BOTTLE, PLASTIC in 1 PACKAGE / 355 mL in 1 BOTTLE, PLASTIC (0363-9913-02)

* 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 0363-9913-99 identifies a specific commercial package of 2 bottle, plastic in 1 carton / 355 ml in 1 bottle, plastic (0363-9913-02) of Cold And Flu Night, a human over the counter drug labeled by Walgreen Company. This solution is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; doxylamine succinate 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 November 14, 2022. The current certification is valid through December 31, 2026.

How is this Walgreen Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363991399. 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 (4-4-2)
0363-9913-99
11-Digit CMS (5-4-2)
00363-9913-99

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