Loratadine Tablet
Product Images NDC 82725-0142

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Loratadine (NDC 82725-0142). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cabinet Health P.b.c., 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

Label100k (Label100k)

Packaging label for Loratadine Tablets, USP 10 mg oral tablets by Cabinet Health P.B.C. The label highlights the product as an antihistamine for indoor and outdoor allergies with 24-hour relief of sneezing, runny nose, itchy watery eyes, and itchy throat or nose. It states non-drowsy when taken as directed and indicates a package size of 100,000 tablets.*

FDA Label Image

Label10k (Label10k)

Drug Facts panel for Loratadine Tablets, USP 10 mg, an oral antihistamine tablet for relief of symptoms from indoor and outdoor allergies. The label includes active ingredient, uses, warnings, directions, storage instructions, inactive ingredients, and contact information. It specifies 10,000 tablets and highlights non-drowsy use when taken as directed.*

FDA Label Image

Label80 (Label80)

Drug Facts panel for Loratadine Tablets, USP 10 mg describes the active ingredient as Loratadine USP 10 mg, an antihistamine. It lists uses such as relieving sneezing, runny nose, itchy watery eyes, and itchy throat or nose due to allergies. Warnings, directions for use, storage instructions, inactive ingredients, and contact information for questions are included. The label states the package contains 8,000 tablets and is manufactured for Cabinet Health P.B.C.*

FDA Label Image

Label96 (Label96)

Drug Facts panel for Loratadine Tablets USP 10 mg, an antihistamine for indoor and outdoor allergies. It lists uses, warnings, directions, inactive ingredients, and storage instructions. The panel includes cautions about allergic reactions, liver or kidney disease, and advises consulting a doctor for children under 6 or patients with certain conditions. Manufactured by Unique Pharmaceutical Laboratories, repackaged for Cabinet Health P.B.C.*

* 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.