Allegra Allergy
Product Images NDC 50090-1235

3 FDA label images from A-s Medication Solutions · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Allegra Allergy (NDC 50090-1235). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Label Image (Lbl500901234)

Label Image (Lbl500901234)
Allegra Allergy 180 mg tablets packaging label showing the active ingredient fexofenadine, marketed by A-S Medication Solutions. The label indicates an oral allergy relief medication, non-drowsy, with 30 tablets per container. Storage instructions specify maintaining temperature between 68 to 77 degrees Fahrenheit and protecting from excessive moisture.*
FDA Label Image

Lbl500901235

Lbl500901235
Allegra Allergy 180 mg 12-hour Indoor/Outdoor Allergy Relief non-drowsy tablets package label by A-S Medication Solutions. The label indicates each tablet contains 60 mg antihistamine fexofenadine HCl, with 12 tablets in the package. Storage instructions advise keeping at 68°F to 77°F and protecting from excessive moisture.*
FDA Label Image

Lbl500901845

Lbl500901845
Label for Allegra Allergy 180 mg tablets by A-S Medication Solutions. The label includes the product name, strength, quantity (1 box of 30 tablets), storage instructions to keep between 68 to 77 degrees F and protect from excessive moisture, and the distributor's address in Libertyville, Illinois.*

* 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.