Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride Tablet, Extended Release
Product Images NDC 41415-995

2 FDA label images from Publix Super Markets, 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 Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride (NDC 41415-995). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Publix Super Markets, 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

Principal Display Panel (20 Tablet Blister Pack Carton)

Principal Display Panel (20 Tablet Blister Pack Carton)
Packaging label for AllergyReliefD extended-release tablets by Publix Super Markets, Inc. Contains fexofenadine hydrochloride 60 mg and pseudoephedrine hydrochloride 120 mg per tablet. The label highlights 12-hour, non-drowsy allergy and congestion relief, with 20 tablets per package. Includes Drug Facts, directions, warnings, inactive ingredients, and barcodes, as well as branding and product usage information.*
FDA Label Image

Principal Display Panel (30 Tablet Blister Pack Carton)

Principal Display Panel (30 Tablet Blister Pack Carton)
Packaging label for Publix allergyreliefD extended-release tablets containing fexofenadine HCl 60 mg and pseudoephedrine HCl 120 mg. The oral tablet is a 12-hour, non-drowsy nasal decongestant and antihistamine product indicated for allergy and congestion relief. The package contains 30 tablets and highlights original prescription strength with dosing and safety information.*

* 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.