Fexofenadine Hydrochloride Suspension
Product Images NDC 58602-426

View Photos of 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 Fexofenadine Hydrochloride (NDC 58602-426). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth Llc, 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

Package Label-principal Display Panel (8 FL OZ Container Label (240 mL Bottle))

Package Label-principal Display Panel (8 FL OZ Container Label (240 mL Bottle))
Label for Fexofenadine Hydrochloride Oral Suspension 30 mg/5 mL by Aurohealth LLC, an antihistamine for children ages 2 years and older. It is a non-drowsy, berry-flavored 8 fl. oz. (240 mL) bottle providing indoor/outdoor allergy relief. The label highlights dosing instructions, warnings, inactive ingredients, and storage conditions.*
FDA Label Image

Package Label-principal Display Panel (8 FL OZ Carton Container Label (240 mL Bottle))

Package Label-principal Display Panel (8 FL OZ Carton Container Label (240 mL Bottle))
Packaging label for Children's Fexofenadine Hydrochloride Oral Suspension 30 mg/5 mL, an antihistamine suspension in berry flavor by Aurohealth LLC. The label indicates it is non-drowsy, for ages 2 years and older, and provides 12-hour relief for indoor/outdoor allergy symptoms including sneezing, runny nose, itchy watery eyes, and itchy nose or throat. The 8 fl. oz. (240 mL) bottle is alcohol and dye free and includes an image of the dosing cup.*

* 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.