Loratadine Tablet
Product Images NDC 68001-438

3 FDA label images from Bluepoint Laboratories · 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 Loratadine (NDC 68001-438). 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

10mg Blister (10mg Blister)

10mg Blister (10mg Blister)
Packaging label for Loratadine Tablets USP 10 mg oral tablets by BluePoint Laboratories. The carton states it contains 100 tablets of loratadine, an antihistamine used for indoor and outdoor allergy relief. It includes drug facts, directions, warnings, and inactive ingredients. The labeler is BluePoint Laboratories, and the product NDC is 68001-438.*
FDA Label Image

10mg Bottle Label (10mg Bottle Label)

10mg Bottle Label (10mg Bottle Label)
Loratadine Tablets, USP 10 mg oral tablets by BluePoint Laboratories. The label highlights the antihistamine's use for indoor and outdoor allergies, offering non-drowsy 24-hour relief for sneezing, runny nose, itchy watery eyes, and itchy throat or nose. The package contains 100 tablets and includes warning and usage information.*
FDA Label Image

Loratadine Tablets Usp 10mg Bottle Carton

Loratadine Tablets Usp 10mg Bottle Carton
Packaging label for Loratadine Tablets USP 10 mg, an oral antihistamine by BluePoint Laboratories. The label displays product details including 30 tablets per package, indications for indoor and outdoor allergy symptom relief, directions for use, drug facts, inactive ingredients, and storage instructions. The label also includes barcode, lot, and expiration information.*

* 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.