Active Ingredient (In Each Tablet)
Omeprazole 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Company for the product Omeprazole (NDC 0363-6101). 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: Do not use if you are allergic to omeprazole
These may be signs of a serious condition. See you 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).
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
carnauba wax, FD&C blue #1/brilliant blue FCF aluminum lake, hypromellose, hypromellose acetate succinate, lactose monohydrate, menthol, monoethanolamine, sodium lauryl sulfate, sodium starch glycolate, sodium stearate, sodium stearyl fumarate, sucralose, talc, titanium dioxide, triacetin, triethyl citrate
1-800-719-9260
Treats frequent heartburn!
Walgreens
WALGREENS PHARMACIST RECOMMENDED
Compare to Prilosec OTC®
Cool Mint Coated Tablet
Omeprazole
DELAYED RELEASE TABLETS 20 mg / ACID REDUCER
24 HR
42 TABLETS
THREE 14-DAY COURSES OF TREATMENT
MAY TAKE 1 TO 4 DAYS FOR FULL EFFECT
SWALLOW – DO NOT CHEW
ACTUAL SIZE
Cool Mint coated tablet
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