Package Label-principal Display Panel (20 mg (25 Tablets Container Label))
Famotidine Tablet, Film Coated
Product Images NDC 55315-435
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Product Visual Gallery
This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 55315-435). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Fred's, 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
Package Label-principal Display Panel (20 mg (25 Tablets Container Carton Label))
This is an information sheet for a medication called MAXIMUM STRENGTH Acid Reducer which contains Famotidine 20 mg. The medication relieves heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages. The medication should not be used if there are signs of a serious condition such as trouble or pain swallowing, vomiting with blood, or black stools. The medication should also not be used if the patient has kidney disease or has been experiencing heartburn for over 3 months or experiencing chest pain or shoulder pain with shortness of breath, sweating; pain spreading to arms, neck, or shoulders; or frequent chest pain or wheezing. The medication should not be taken for more than 14 days, and a health professional should be consulted before use if pregnant or breastfeeding. The medication should be stored at 20°C to 25°C and out of reach of children. The inactive ingredients include carnauba wax, cornstarch, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, red iron oxide, sodium starch glycolate, talc, titanium dioxide, and yellow iron oxide. For more information, contact 1-855-274-4122.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
