Loratadine Capsule, Liquid Filled
Product Images NDC 25000-021

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Loratadine (NDC 25000-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marksans 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

28 Carton Label

Loratadine 10 mg liquid-filled capsules packaging label by Marksans Pharma Limited. The label highlights non-drowsy properties and relief for indoor and outdoor allergies with 28 capsules per container. It lists active ingredient loratadine 10 mg per capsule and includes usage warnings, directions, and storage information. The label also shows manufacturing details and a barcode.*

FDA Label Image

600s Carton Label

Packaging label for Loratadine capsules, liquid-filled, 10 mg strength by Marksans Pharma Limited. The label highlights non-drowsy 24-hour relief for indoor and outdoor allergies, including sneezing, runny nose, itchy watery eyes, and itchy throat or nose. The package contains 600 capsules.*

FDA Label Image

New 3x10 Carton

Loratadine 10 mg liquid-filled capsules packaging label by Marksans Pharma Limited shows a 30-count carton. The label emphasizes non-drowsy 24-hour allergy relief, indicating use for indoor and outdoor allergies including sneezing, runny nose, itchy watery eyes, and itchy throat or nose. The design features the product name prominently with purple and blue gradient colors, the NDC 25000-021-36, and drug facts panel instructions.*

* 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.