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  5. NDC Package Code: 50066-517-25 Tukol Max Action Severe Congestion And Cough

NDC Package 50066-517-25 Tukol Max Action Severe Congestion And Cough

Dextromethorphan Hbr,Guaifenesin,Phenylephrine Hcl Liquid 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:
50066-517-25
Package Description:
177 mL in 1 BOTTLE
Product Code:
50066-517
Proprietary Name:
Tukol Max Action Severe Congestion And Cough
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than 6 doses in any 24 hoursUse dose cup providedAge                                                       DoseAdults and children12 years and older                                20 mL every 4 hoursChildren under 12 years of age            Do not use
11-Digit NDC Billing Format:
50066051725
NDC to RxNorm Crosswalk:
  • RxCUI: 1043543 - dextromethorphan HBr 5 MG / guaiFENesin 100 MG / phenylephrine HCl 2.5 MG in 5 mL Oral Solution
  • RxCUI: 1043543 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1043543 - dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
  • RxCUI: 1043543 - dextromethorphan HBr 5 MG / guaifenesin 100 MG / phenylephrine HCl 2.5 MG per 5 ML Oral Solution
Product Type:
Human Otc Drug
Labeler Name:
Genomma Lab Usa, Inc
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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:
12-16-2016
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 50066-517-25?

The NDC Packaged Code 50066-517-25 is assigned to a package of 177 ml in 1 bottle of Tukol Max Action Severe Congestion And Cough, a human over the counter drug labeled by Genomma Lab Usa, Inc. The product's dosage form is liquid and is administered via oral form.

Is NDC 50066-517 included in the NDC Directory?

Yes, Tukol Max Action Severe Congestion And Cough with product code 50066-517 is active and included in the NDC Directory. The product was first marketed by Genomma Lab Usa, Inc on December 16, 2016 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 50066-517-25?

The 11-digit format is 50066051725. 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
5-3-250066-517-255-4-250066-0517-25