Loratadine Tablet
Product Images NDC 58602-831

2 FDA label images from Aurohealth Llc · 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 (NDC 58602-831). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth Llc, 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

Package Label-principal Display Panel (10 mg (45 Tablets Bottle))

Package Label-principal Display Panel (10 mg (45 Tablets Bottle))
The label for Loratadine Tablets USP 10 mg by AuroHealth features the proprietary name Allergy Relief and includes indications for indoor and outdoor allergy symptoms such as sneezing, runny nose, and itchy, watery eyes. The label states the product is non-drowsy and provides 24-hour relief. The package contains 45 tablets. The label also includes drug facts, storage instructions, and manufacturer information from AuroHealth LLC in NJ, USA.*
FDA Label Image

Fig2 (Loratadine Fig2)

Fig2 (Loratadine Fig2)
Packaging label for Loratadine 10 mg tablets, an antihistamine by Aurohealth LLC under the Primary Health brand. The front shows 45 tablets with indications for allergy relief, including sneezing, runny nose, itchy/watery eyes, and itchy throat or nose. The label highlights non-drowsy, 24-hour relief for indoor and outdoor allergies. Drug Facts panels on the sides provide active ingredient, uses, warnings, directions, and inactive ingredients. The package includes a barcode and distribution 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.