Fexofenadine Hydrochloride Suspension
Product Images NDC 58602-427

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 58602-427). 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.(240 mL Bottle) Container Label)

Package Label-principal Display Panel (8 fl. oz.(240 mL Bottle) Container Label)
Label for Children's Fexofenadine Hydrochloride Oral Suspension, 30 mg/5 mL, raspberry flavored, non-drowsy antihistamine by Aurohealth LLC. The 8 fl. oz. (240 mL) bottle offers indoor/outdoor allergy relief for ages 2 years and older, with included dosing cup and alcohol- and dye-free formulation. The label includes dosage instructions, warnings, active ingredient info, and manufacturer contact details.*
FDA Label Image

Package Label-principal Display Panel (8 fl. oz. (240 mL Bottle) Carton Container Label)

Package Label-principal Display Panel (8 fl. oz. (240 mL Bottle) Carton Container Label)
Packaging label for Children's Fexofenadine Hydrochloride Oral Suspension 30 mg/5 mL, raspberry flavor, 8 fl. oz. (240 mL) liquid. The label shows the product as a non-drowsy antihistamine for indoor and outdoor allergy relief for ages 2 years and older, distributed by Aurohealth LLC. It highlights the 12-hour relief duration and features dosing instructions with an enclosed dosing cup image.*

* 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.