Loratadine Tablet
Product Images NDC 51079-246

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Loratadine (NDC 51079-246). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional Inc., 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 Tablets, Usp 10 mg Carton Label (Image 01)

Loratadine 10 mg tablets, USP, oral antihistamine by Mylan Institutional Inc., NDC 51079-246-20. The label indicates original prescription strength for indoor and outdoor allergies with 24-hour relief. The package contains 100 tablets (10 x 10). Additional information includes tamper-evident warnings and inactive ingredients such as corn starch and lactose monohydrate.*

FDA Label Image

Outer Carton Label (Image 02)

Blue unit dose packaging label for Loratadine 10 mg oral tablet by Mylan Institutional Inc. The front includes a white box with the text 'UNIT-DOSE' and a window area presumably for lot number and expiration date. The label notes that the package is not child resistant, for institutional use only, light-resistant, and shows storage warnings. The back has a label area with a QR code and placeholder text for serial number, lot number, and expiration date.*

* 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.