Maximum Strength Daytime Severe And Nighttime Cold And Flu
NDC Package 11673-339-01

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.

Maximum Strength Daytime Severe And Nighttime Cold And Flu is nighttimedo not take more than directed (see overdose warning) do not take more than 6 doses in any 24-hour periodmeasure only with dosing cup provided. Marketed by Target Corporation, this product is identified by NDC 11673-339 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
11673-339-01
Package Description
1 KIT in 1 KIT * 177 mL in 1 BOTTLE, PLASTIC * 177 mL in 1 BOTTLE, PLASTIC
Product Code
11673-339
11-Digit Billing Format
11673033901
RxNorm Crosswalk
  • RxCUI: 1116572 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaiFENesin 400 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution
  • RxCUI: 1116572 - acetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1116572 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG per 10 ML Oral Solution
  • RxCUI: 1116572 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine hydrochloride 10 MG per 20 ML Oral Solution
  • RxCUI: 1116572 - APAP 32.5 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / Guaifenesin 20 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Maximum Strength Daytime Severe And Nighttime Cold And Flu
Dosage Form
-
Usage Information
Nighttimedo not take more than directed (see overdose warning) do not take more than 6 doses in any 24-hour periodmeasure only with dosing cup provided. Do not use any other dosing devicekeep dosing cup with productmL = mililiterdose as follows or as directed by a doctoradults and children 12 years and older: 20 mL every 4 hours while symptoms lastchildren under 12 years of age: do not useDaytimedo not take more than directed (see Overdose warning)do not take more than 6 doses in any 24-hours periodmeasure only with dosing cup provided. Do not use any other dosing device.dose as follows or as directed by a doctor keep dosing cup with product mL = milliliteradults and children 12 years of age and older: 20 mL every 4 hourschildren under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
Target Corporation
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-01-2024
Listing Expiration
12-31-2024
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 11673-339-01 identifies a specific commercial package of 1 kit in 1 kit * 177 ml in 1 bottle, plastic * 177 ml in 1 bottle, plastic of Maximum Strength Daytime Severe And Nighttime Cold And Flu, labeled by Target Corporation. 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 Target Corporation on May 01, 2024. The current certification is valid through December 31, 2024.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673033901. 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)
11673-339-01
11-Digit CMS (5-4-2)
11673-0339-01

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