Tukol Max Action Cold And Flu Nighttime Relief Syrup
NDC Package 50066-520-06

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

Package Information

Tukol Max Action Cold And Flu Nighttime Relief (acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate) syrups is do not exceed 4 doses per 24 hours (see Overdose warning).use the dosing cup provided and keep cup with product.mL = milliliteragedoseadults & children 12 yrs & over30 mL every 6 hrschildren under 12 years of agedo not usewhen using day time and night time products, carefully read each label to ensure correct dosing. This formulation utilizes a syrup delivery system. Marketed by Genomma Lab Usa, this product is identified by NDC 50066-520 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
50066-520-06
Package Description
1 BOTTLE, PLASTIC in 1 CARTON / 177 mL in 1 BOTTLE, PLASTIC
Product Code
50066-520
11-Digit Billing Format
50066052006

Clinical Specifications

Proprietary Name
Tukol Max Action Cold And Flu Nighttime Relief
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, And Doxylamine Succinate
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Doxylamine Succinate
Dosage Form
Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not exceed 4 doses per 24 hours (see Overdose warning).use the dosing cup provided and keep cup with product.mL = milliliteragedoseadults & children 12 yrs & over30 mL every 6 hrschildren under 12 years of agedo not usewhen using day time and night time products, carefully read each label to ensure correct dosing.

Regulatory & Marketing

Labeler Name
Genomma Lab Usa
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-30-2026
Listing Expiration
12-31-2027
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 50066-520-06 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 177 ml in 1 bottle, plastic of Tukol Max Action Cold And Flu Nighttime Relief, a human over the counter drug labeled by Genomma Lab Usa. This syrup is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; doxylamine succinate 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 Genomma Lab Usa on July 30, 2026. The current certification is valid through December 31, 2027.

How is this Genomma Lab Usa product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50066052006. 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)
50066-520-06
11-Digit CMS (5-4-2)
50066-0520-06

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