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  5. NDC Package Code: 82442-694-04 Up And Up Daytime Childrens Multi Symptom Cold

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

Dextromethorphan Hydrobromide,Guaifenesin,And Phenylephrine Hydrochloride Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
82442-694-04
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code:
82442-694
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
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
11-Digit NDC Billing Format:
82442069404
Product Type:
Human Otc Drug
Labeler Name:
Target Corporation
Dosage Form:
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-19-2024
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 82442-694-04?

The NDC Packaged Code 82442-694-04 is assigned to a 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. The product's dosage form is suspension and is administered via oral form.

Is NDC 82442-694 included in the NDC Directory?

Yes, Up And Up Daytime Childrens Multi Symptom Cold with product code 82442-694 is active and included in the NDC Directory. The product was first marketed by Target Corporation on July 19, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 82442-694-04?

The 11-digit format is 82442069404. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-282442-694-045-4-282442-0694-04