Giltuss Tr Tablet
Product Images NDC 58552-355

2 FDA label images from Gil Pharmaceutical Corp · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Giltuss Tr (NDC 58552-355). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gil Pharmaceutical Corp, 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

Image Description (Giltuss 100s Bottle Label)

Image Description (Giltuss 100s Bottle Label)
Drug Facts panel for Giltuss TR tablets showing active ingredients: Dextromethorphan HBr 29 mg, Guaifenesin 390 mg, and Phenylephrine HCl 10 mg per tablet. Includes product uses, warnings, directions by age group, inactive ingredients, and storage instructions. Contact information for Gil Pharmaceutical Corp in Ponce, Puerto Rico is provided.*
FDA Label Image

Image Description (Giltuss 100s Label)

Image Description (Giltuss 100s Label)
Drug Facts panels for Giltuss TR Total Release tablets, containing active ingredients Dextromethorphan HBr 29 mg (cough suppressant), Guaifenesin 390 mg (expectorant), and Phenylephrine HCl 10 mg (nasal decongestant). The panels detail uses, warnings, directions, inactive ingredients, and manufacturer information from Gil Pharmaceutical Corp. The label includes instructions for adults and children, precautions, and storage information. This labeling indicates the product NDC is 58552-355-02 and emphasizes typical cold and allergy symptom relief.*

* 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.