Loratadine Solution
Product Images NDC 68001-449

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Loratadine (NDC 68001-449). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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 Os Carton (Loratadine Os Carton Rev 0620)

Loratadine Oral Solution USP 5 mg/5 mL by BluePoint Laboratories. This grape-flavored liquid oral antihistamine is indicated for relief of indoor and outdoor allergy symptoms such as sneezing, runny nose, itchy watery eyes, and itchy throat or nose. The package includes dosing instructions, safety warnings, and a dosing cup for accurate measurement. The label notes it is non-drowsy, sugar-free, alcohol-free, and suitable for use in children aged 2 years and older.*

FDA Label Image

Loratadine Os Label (Loratadine Os Label Rev 0620)

Loratadine Oral Solution USP 5 mg/5 mL in a 4 fl oz (120 mL) bottle produced by BluePoint Laboratories. This antihistamine solution is designed for ages 2 years and older and provides 24-hour relief of indoor and outdoor allergy symptoms such as sneezing, runny nose, itchy watery eyes, and itchy throat or nose. The label indicates it is non-drowsy, dye-free, sugar-free, alcohol-free, and grape-flavored. The product NDC is 68001-449-98.*

* 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.