Benadryl Ultra Tab Tablet, Film Coated
Product Images NDC 50269-226

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Benadryl Ultra Tab (NDC 50269-226). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jc World Bell Wholesale Co., 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.

Product Images & Figures Index

FDA Label Image

Label2 (Label2)

Label2 (Label2)
This is a drug facts sheet for Benadryl allergy medicine. The active ingredient is Diphenhydramine HCI 25mg antihistamine. It temporarily relieves symptoms due to upper respiratory allergies or common cold such as runny nose, sneezing, itchy, watery eyes, itching of the nose or throat. The user should not use it to make a child sleepy nor should it be used in combination with another product containing diphenhydramine. It should also not be used if the patient has a breathing problem such as emphysema, chronic bronchitis, or glaucoma. This product can cause drowsiness, and alcohol, sedatives, and tranquilizers can increase this effect. It should be used with caution when driving or operating machinery. It should not be taken more than six times in 24 hours. The drug contains croscarmellose sodium, carnauba wax, aluminum, and D&C red no. 27 as inactive ingredients. This drug is distributed by Johnson & Johnson Consumer Inc., and it is repackaged with permission by JC World Bell Wholesale Company.*

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