Active Ingredient (In Each Tablet)
Omeprazole 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Meijer Distribution Inc for the product Omeprazole (NDC 41250-915). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, use, warnings, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Omeprazole 20 mg
Acid reducer
Allergy alert: Do not use if you are allergic to omeprazole
if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
taking
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
children under 18 years of age: ask a doctor. Heartburn in children may sometimes be caused by a serious condition.
carnauba wax, ferric oxide red, ferric oxide yellow, hypromellose, hypromellose acetate succinate, lactose monohydrate, monoethanolamine, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, sodium stearate, sodium stearyl fumarate, talc, titanium dioxide, triethyl citrate
1-800-719-9260
FDA Approved
Omeprazole Delayed Release Tablets 20 mg
Acid Reducer
Treats Frequent Heartburn!
Occurring 2 Or More Days A Week
Actual Size
42 Tablets
Three 14-day courses of treatment
* Please review the disclaimer below.