Active Ingredient (In Each Tablet)
Omeprazole 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Topco Associates Llc for the product Topcare Omeprazole (NDC 76162-470). 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
1-888-423-0139
TopCare® health
VALUE PACK! THREE-14 TABLET BOTTLES
Omeprazole DELAYED RELEASE TABLETS 20 mg
COMPARE TO PRILOSEC OTC®
3 Bottles Inside
ACID REDUCER
24 HR
Treats Frequent Heartburn!
COOL MINT COATED TABLET
SWALLOW – DO NOT CHEW
42 TABLETS
THREE 14-DAY COURSES OF TREATMENT • MAY TAKE 1 TO 4 DAYS FOR FULL EFFECT
actual size
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