Loratadine Odt
Product Images NDC 41250-527

2 FDA label images from Meijer Distribution, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Loratadine Odt (NDC 41250-527). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meijer Distribution, 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

This Is The 24 Count Blister Carton Label For Meijer Loratadine Odt (alavert). (Loraodt Alavert)

This Is The 24 Count Blister Carton Label For Meijer Loratadine Odt (alavert). (Loraodt Alavert)
The packaging label for Meijer Loratadine ODT Allergy Relief displays loratadine orally disintegrating tablets, 10 mg strength, in a mint flavor. It emphasizes non-drowsy, 24-hour allergy relief for adults and children six years and older. The label highlights features such as no water needed and melting in the mouth, with 24 tablets per package. It notes relief for indoor and outdoor allergies and lists common symptoms addressed by the medication.*
FDA Label Image

This Is The 30 Count Blister Carton Label For Meijer Loratadine Odt, Claritin Like. (Loraodt Claritin)

This Is The 30 Count Blister Carton Label For Meijer Loratadine Odt, Claritin Like. (Loraodt Claritin)
Box packaging for Meijer Allergy Relief Loratadine Orally Disintegrating Tablets, 10 mg, antihistamine, containing 30 orally disintegrating tablets. The label highlights 24-hour non-drowsy allergy relief for adults and children six years and older, with no water needed. The product is distributed by Meijer Distribution, Inc., Grand Rapids, MI.*

* 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.