Active Ingredient (In Each Tablet)
Omeprazole 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Up And Up Omeprazole (NDC 11673-915). 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 taking, 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.
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)
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
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omeprazole delayed release tablets 20 mg
acid reducer
ACTUAL SIZE
14 TABLETS
treats frequent heartburn!
occurring 2 or more days a week
1 bottle inside
14 TABLETS
ONE 14-DAY COURSE OF TREATMENT
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