Tricode
Product Images NDC 60575-414

2 FDA label images from Respa Pharmaceuticals, Inc. · 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 Tricode (NDC 60575-414). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Respa Pharmaceuticals, 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.

Product Images & Figures Index

FDA Label Image

Tricode Gf Packaging (Mm1)

Tricode Gf Packaging (Mm1)
Tricode GF 60575-414-16 bottle label by Respa Pharmaceuticals, Inc., showing a liquid cough suppressant and expectorant nasal decongestant. Each 5 mL contains 8 mg Codeine Phosphate, 200 mg Guaifenesin, and 30 mg Pseudoephedrine HCl. The label highlights grape flavor, dye-free, sugar-free, alcohol-free, gluten-free, and Rx only status. The drug facts panel lists active ingredients, uses, warnings, and storage instructions on a blue and white background with barcode and manufacturer details from Addison, IL.*
FDA Label Image

Tricode Gf Packaging (Mm2)

Tricode Gf Packaging (Mm2)
This image shows the Drug Facts panel continuing with warnings about trouble urinating due to an enlarged prostate gland, instructions to stop use and ask a doctor if certain symptoms occur, and precautions for pregnant or breastfeeding women. It includes directions for dosing by age group and emphasizes not exceeding recommended dosages. The panel also lists storage instructions, inactive ingredients such as bitter mask and citric acid, a customer service phone number, and identifies Respa Pharmaceuticals, Inc. as the manufacturer in Addison, IL.*

* 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.