Dye-free Loratadine Tablet, Chewable
Product Images NDC 51660-755

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Dye-free Loratadine (NDC 51660-755). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ohm Laboratories 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

Carton (Ohm Lora Chew Tab Grape 10mg 24ct Blister Carton)

Carton (Ohm Lora Chew Tab Grape 10mg 24ct Blister Carton)
This is a description of Loratadine Chewable Tablets, an antihistamine medication that helps relieve symptoms of hay fever and other upper respiratory allergies. The chewable tablets are meant to be chewed before swallowing. Each tablet contains 10 mg of Loratadine as the active ingredient. It provides relief from symptoms such as runny nose, itchy/watery eyes, and sneezing associated with allergies. The recommended dosage for adults and children 6 years and older is to chew 1 tablet daily. The tablets should not be crushed but chewed completely before swallowing. The product is not to be used if allergic to any of its components. For individuals with liver or kidney issues, consultation with a doctor is advised before use. The tablets should not be taken more than directed to avoid drowsiness. If experiencing an allergic reaction, medical attention should be sought immediately. The product contains inactive ingredients such as aspartame, citric acid, and magnesium stearate. The product should be kept out of reach of children and in case of an overdose, medical help should be sought. The carton contains important information including the expiration date. For any questions or concerns, a toll-free helpline is available.*

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