Trispec Pse Cough Suppressant Expectorant Nasal Decongestant Grape Flavor
Product Images NDC 58238-228

2 FDA label images from Deliz 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 Trispec Pse Cough Suppressant Expectorant Nasal Decongestant Grape Flavor (NDC 58238-228). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Deliz 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

Trispec Pse Labeling 1 (Trispec Pse Labeling 1)

Trispec Pse Labeling 1 (Trispec Pse Labeling 1)
Label for TRISPEC PSE Cough Suppressant Expectorant Nasal Decongestant Grape Flavor by Deliz Pharmaceutical Corp. The product is a 4 fl oz (118 ml) liquid with grape flavor, labeled as sugar, alcohol, dye, and gluten free. Active ingredients include Dextromethorphan HBr 10 mg, Guaifenesin USP 187 mg, and Phenylephrine HCl USP 30 mg per 10 ml. The label provides drug facts, purpose, uses, and a barcode with NDC 58238-228-04.*
FDA Label Image

Trispec Pse Labeling 2 (Trispec Pse Labeling 2)

Trispec Pse Labeling 2 (Trispec Pse Labeling 2)
Drug Facts panels continuing warnings, directions, dosage limits, other information, inactive ingredients, and a contact number for the product TRISPEC PSE Cough Suppressant Expectorant Nasal Decongestant GRAPE Flavor by Deliz Pharmaceutical Corp. The text covers cautions for use with certain conditions, dosage instructions for different age groups, storage instructions, and inactive ingredients including bitter mask and citric acid.*

* 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.