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 41250-401). 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 if you have:, 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:
If an allergic reaction occurs, stop use and seek medical help right away.
These may be signs of a serious condition. See your doctor.
taking a prescription drug. Acid reducers may interact with certain prescription drugs.
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).
benzyl alcohol, carmine, carnauba wax, FD&C blue #2/indigo carmine aluminum lake, flavor, hypromellose, hypromellose acetate succinate, lactose monohydrate, menthol, modified starch, monoethanolamine, polyethylene glycol 3350, sodium lauryl sulfate, sodium starch glycolate, sodium stearate, sodium stearyl fumarate, sucralose, talc, titanium dioxide, triacetin, triethyl citrate
meijer®
Omeprazole
Delayed Release Tablets, 20 mg | Acid Reducer
COMPARE TO PRILOSEC OTC®
24 HR
TREATS FREQUENT HEARTBURN!
WILDBERRY MINT COATED TABLET
SWALLOW – DO NOT CHEW
Actual Size
42 TABLETS
THREE 14-DAY COURSES OF TREATMENT
MAY TAKE 1 TO 4 DAYS FOR FULL EFFECT
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