Tukol Max Action Cold, Sore Throat And Cough Liquid
Product Images NDC 50066-516

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Tukol Max Action Cold, Sore Throat And Cough (NDC 50066-516). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Genomma Lab Usa, Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Aptapharma Tukol Maxstrengthcold 516 (Aptapharma Tukol Maxstrength Cold 516)

Aptapharma Tukol Maxstrengthcold 516 (Aptapharma Tukol Maxstrength Cold 516)
Packaged label for Tukol MAX ACTION Cold, Sore Throat and Cough oral liquid by Genomma Lab USA, Inc. Contains active ingredients acetaminophen, dextromethorphan HBr, guaifenesin, and phenylephrine HCl in specific mg per 20mL dosages. The 6 fl oz (177 mL) bottle label highlights relief from fever, headache, nasal congestion, mucus, cough, and provides warnings and directions for use in adults and children 12 years and older.*
FDA Label Image

Aptapharma Tukol Maxstrengthcold 516-1 (Aptapharma Tukol Maxstrengthcold 516 1)

Aptapharma Tukol Maxstrengthcold 516-1 (Aptapharma Tukol Maxstrengthcold 516 1)
Tukol MAX ACTION Cold, Sore Throat and Cough oral liquid, 6 fl oz (177 ml) by Genomma Lab USA, Inc. The label indicates the product contains acetaminophen, dextromethorphan HBr, guaifenesin, and phenylephrine HCl, with strength details on the label. It is marketed for relief of cold, sore throat, and cough symptoms including fever, headache, nasal congestion, and mucus loosening. The packaging is bilingual in English and Spanish, highlighting the maximum strength formula.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.