Fexofenadine Hydrochloride
Product Images NDC 58602-710

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fexofenadine Hydrochloride (NDC 58602-710). 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

Fexo Fig3

Packaging label for Fexofenadine Hydrochloride Tablets USP, 60 mg by Aurohealth LLC. The label states it is for indoor and outdoor allergies, with 12 tablets per package. It highlights non-drowsy relief for sneezing, runny nose, itchy watery eyes, and itchy nose or throat. The label includes drug facts with active and inactive ingredients, directions, warnings, and contact information.*

FDA Label Image

Principal Display Panel-180 mg-90s Count (Fexofenadine Fig1)

Packaging label for Fexofenadine Hydrochloride Tablets USP 180 mg by Aurohealth LLC. The carton states 90 tablets and indicates the product is for allergy relief, specifically indoor and outdoor allergies. The label features active ingredient details, warnings, directions, and a Drug Facts panel. The design uses a blue, orange, and purple color scheme with curved lines and includes the labeler name and barcode.*

FDA Label Image

Fexofenadinehcl (Fexofenadinehcl)

Packaging label for Fexofenadine Hydrochloride Tablets USP, 60 mg, antihistamine by Aurohealth LLC. The label highlights allergy relief for indoor and outdoor allergies, with 500 tablets in the package. It notes the product is non-drowsy, provides 12-hour relief, and treats symptoms like sneezing, runny nose, itchy/watery eyes, and itchy nose or throat.*

* 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.