Sunmark Loratadine Odt
Product Images NDC 49348-930

2 FDA label images from Sunmark · 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 Sunmark Loratadine Odt (NDC 49348-930). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunmark, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

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

This Is The 24 Count Blister Carton Label For Sunmark Loratadine Odt (alavert). (Lora Alavert)
Sunmark Loratadine Orally Disintegrating Tablets 10 mg allergy relief packaging label showing 24 orally disintegrating tablets. The label highlights non-drowsy antihistamine for adults and children six years and older, providing 24-hour relief of indoor and outdoor allergy symptoms such as sneezing, runny nose, and itchy watery eyes. The package includes directions, warnings, drug facts, and manufacturer information from Sunmark/McKesson.*
FDA Label Image

This Is The 10 Count Blister Carton Label For Sunmark Loratadine Odt, 10 mg. (Lora Odt)

This Is The 10 Count Blister Carton Label For Sunmark Loratadine Odt, 10 mg. (Lora Odt)
Sunmark Loratadine ODT 10 mg orally disintegrating tablets packaging label. The label indicates indication for allergy relief, non-drowsy formula, and use for adults and children six years and older. Contains 10 tablets. The label features dosage form, strength, and directions for indoor and outdoor allergy symptom relief. Distributed by McKesson, with a barcode and comparison to Claritin Reditabs.*

* 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.