Loratadine Allergy Relief Tablet
Product Images NDC 55289-728

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Loratadine Allergy Relief (NDC 55289-728). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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.

FDA Label Image

55289728 Label (55289728)

Drug Facts panel for Loratadine Allergy Relief Tablets USP 10 mg, showing active ingredient loratadine as an antihistamine. Includes warnings on allergic reactions, liver/kidney disease, pregnancy, and overdose. Directions specify 1 tablet daily for adults and children over 6 years, with instructions to ask a doctor for younger children or those with liver/kidney disease. Storage instructions and inactive ingredients are also listed. Packaged by PD-Rx Pharmaceuticals, Inc.*

* 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.