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  5. NDC Package Code: 70000-0739-1 Leader Tussin Cf

NDC Package 70000-0739-1 Leader Tussin Cf

Acetaminophen,Dextromethorphan Hydrobromide,Guaifenesin Solution 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:
70000-0739-1
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code:
70000-0739
Proprietary Name:
Leader Tussin Cf
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
•do not take more than 5 doses in any 24-hour period•do not exceed recommended dosage. Taking more than the recommended dose (overdose) may cause serious liver damage.•measure only with dosing cup provided•keep dosing cup with product•mL = milliliter•this adult product is not intended for use in children under 12 years of age agedoseadults and children12 years and over20 mL every 4 hourschildren under 12 yearsdo not use
11-Digit NDC Billing Format:
70000073901
Product Type:
Human Otc Drug
Labeler Name:
Cardinal Health 110, Llc. Dba Leader
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(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:
09-30-2025
Listing Expiration Date:
12-31-2026
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 70000-0739-1?

The NDC Packaged Code 70000-0739-1 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle of Leader Tussin Cf, a human over the counter drug labeled by Cardinal Health 110, Llc. Dba Leader. The product's dosage form is solution and is administered via oral form.

Is NDC 70000-0739 included in the NDC Directory?

Yes, Leader Tussin Cf with product code 70000-0739 is active and included in the NDC Directory. The product was first marketed by Cardinal Health 110, Llc. Dba Leader on September 30, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70000-0739-1?

The 11-digit format is 70000073901. 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 5-4-1 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
5-4-170000-0739-15-4-270000-0739-01