Loratadine Tablet, Orally Disintegrating
Product Images NDC 72888-029

2 FDA label images from Advagen Pharma Limited · 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 Loratadine (NDC 72888-029). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advagen Pharma Limited, 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

Loratadine-odt-usp-10mg-10count (Loratadine Odt Usp 10mg 10count)

Loratadine-odt-usp-10mg-10count (Loratadine Odt Usp 10mg 10count)
Loratadine 10 mg orally disintegrating tablets label, an antihistamine for relief of indoor and outdoor allergy symptoms such as sneezing, runny nose, and itchy, watery eyes. The label indicates original prescription strength, 10 tablets per package, providing 24-hour relief. Distributed by Advagen Pharma Limited, manufactured by Rubicon Research Private Limited, and includes usage and safety instructions.*
FDA Label Image

Loratadine-odt-usp-10mg-30count (Loratadine Odt Usp 10mg 30count)

Loratadine-odt-usp-10mg-30count (Loratadine Odt Usp 10mg 30count)
Loratadine 10 mg orally disintegrating tablets packaging label showing a blue and white box for allergy relief. It indicates the product is an antihistamine for indoor and outdoor allergies, with 30 tablets per package. The label highlights 24-hour relief and states no water is needed as tablets melt in the mouth. Labeler is Advagen Pharma Limited, and manufacturer is Rubicon Research Private Limited.*

* 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.