Loratadine Tablet
Product Images NDC 82725-0142

View Photos of Packaging, Regulatory Labels, and Product Appearance

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)

Label100k (Label100k)
This text provides details about a medication with the NDC 82725-0142-2 DrugFacts. The medication contains Loratadine USP 10 mg as the active ingredient, which is an antihistamine for relieving symptoms of hay fever or upper respiratory allergies. Key warnings include not using the medication if allergic to it, consulting a doctor before use for individuals with liver or kidney disease, and not exceeding the recommended dosage to avoid drowsiness. The directions for adults and children over 6 years old are described, along with precautions for pregnant or breastfeeding individuals. The medication offers 24-hour relief from symptoms like runny nose, sneezing, itchy throat, or nose, and emphasizes seeking medical help in case of allergic reactions or overdose.*
FDA Label Image

Label10k (Label10k)

Label10k (Label10k)
This text provides information about Loratadine Tablets, USP, a non-drowsy antihistamine for 24-hour relief of allergy symptoms such as sneezing, runny nose, itchy throat or nose, and itchy, watery eyes. It contains 10mg of Loratadine USP per tablet. The medication should not be used if allergic to any of its ingredients. It is recommended to consult a doctor before use if you have liver or kidney disease. Adults and children over 6 years old can take one tablet daily, but not more than one in 24 hours. The tablets should be stored between 20° to 25°C (58°F to 77°F).Inactive ingredients include corn starch, lactose monohydrate, magnesium stearate, and povidone. For any questions or comments, a contact number is provided.*
FDA Label Image

Label80 (Label80)

Label80 (Label80)
This is a description of a medication with the active ingredient Loratadine USP 10 mg, which is used to temporarily relieve symptoms of hay fever or upper respiratory allergies, such as runny nose, sneezing, and itchy, watery eyes. It is a non-drowsy antihistamine providing 24-hour relief. The medication should not be taken more than directed and individuals with liver or kidney disease should consult a doctor before use. The product is recommended for adults and children 6 years and older, with specific dosing instructions provided. Inactive ingredients include corn starch, lactose monohydrate, magnesium stearate, and povidone. Tamper-evident packaging is emphasized for safety. For additional information, contact the manufacturer Cabinet Health PB.C. in Brooklyn, NY.*
FDA Label Image

Label96 (Label96)

Label96 (Label96)
This is a description of Loratadine Tablets, USP, which provide 24-hour non-drowsy relief from allergy symptoms like sneezing, runny nose, itchy throat or nose, and watery eyes. The tablets contain 10 mg of Loratadine USP as the active ingredient. It is recommended for adults and children over 6 years to take one tablet daily, and not more than one tablet in 24 hours. The product should be stored at a temperature between 20° to 25°C (68° to 77°F). In case of allergies or overdose, medical help should be sought immediately.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.