Up And Up Daytime Childrens Multi Symptom Cold Suspension
NDC Package 82442-694-04

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Up And Up Daytime Childrens Multi Symptom Cold (dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride) suspension is do not give more than 6 doses in any 24-hour periodmeasure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctorAgeDosechildren 6 years to under 12 years of age10 mL every 4 hourschildren 4 to under 6 years of age5 mL every 4 hourschildren under 4 years of agedo not use. This formulation utilizes a suspension delivery system. Marketed by Target Corporation, this product is identified by NDC 82442-694 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
82442-694-04
Package Description
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code
82442-694
11-Digit Billing Format
82442069404

Clinical Specifications

Proprietary Name
Up And Up Daytime Childrens Multi Symptom Cold
Non-Proprietary Name
Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride
Substance Name
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Dosage Form
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not give more than 6 doses in any 24-hour periodmeasure only with dosing cup provideddo not use dosing cup with other productsdose as follows or as directed by a doctorAgeDosechildren 6 years to under 12 years of age10 mL every 4 hourschildren 4 to under 6 years of age5 mL every 4 hourschildren under 4 years of agedo not use

Regulatory & Marketing

Labeler Name
Target Corporation
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-19-2024
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 82442-694-04 identifies a specific commercial package of 1 bottle in 1 carton / 118 ml in 1 bottle of Up And Up Daytime Childrens Multi Symptom Cold, a human over the counter drug labeled by Target Corporation. This suspension is formulated for oral use and contains dextromethorphan hydrobromide; guaifenesin; phenylephrine hydrochloride 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 Target Corporation on July 19, 2024. The current certification is valid through December 31, 2026.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82442069404. 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)
82442-694-04
11-Digit CMS (5-4-2)
82442-0694-04

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