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  5. NDC Package Code: 50066-313-06 Tukol Max Action Cold, Flu And Sore Throat

NDC Package 50066-313-06 Tukol Max Action Cold, Flu And Sore Throat

View Billable Units, 11-Digit Format, RxNorm

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.

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:
50066-313-06
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 177 mL in 1 BOTTLE, PLASTIC
Product Code:
50066-313
Proprietary Name:
Tukol Max Action Cold, Flu And Sore Throat
Usage Information:
Do not take more than directedDo not take more than 4 doses in 24 hours.This adult strength product is not intended for use in children under 12 years of ageDose as follows or as directed by a doctorUse dose cup providedagedoseadults and children 12 years and older20 mL every 4 hourschildren under 12 years of agedo not use
11-Digit NDC Billing Format:
50066031306
NDC to 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
    • Labeler Name:
    Genomma Lab Usa
    Sample Package:
    No
    Start Marketing Date:
    12-30-2022
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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 50066-313-06?

    The NDC Packaged Code 50066-313-06 is assigned to a package of 1 bottle, plastic in 1 carton / 177 ml in 1 bottle, plastic of Tukol Max Action Cold, Flu And Sore Throat, labeled by Genomma Lab Usa. The product's dosage form is and is administered via form.

    Is NDC 50066-313 included in the NDC Directory?

    No, Tukol Max Action Cold, Flu And Sore Throat with product code 50066-313 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Genomma Lab Usa on December 30, 2022 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50066-313-06?

    The 11-digit format is 50066031306. 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
    5-3-250066-313-065-4-250066-0313-06