Label: TOPCARE OMEPRAZOLE DELAYED RELEASE- omeprazole tablet, delayed release
- NDC Code(s): 59368-325-01, 59368-325-02
- Packager: Praxis, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated January 1, 2023
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- Official Label (Printer Friendly)
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Active ingredient (in each tablet)Omeprazole 20 mg
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PurposeAcid reducer
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Usetreats frequent heartburn (occurs - 2 or moredays a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect
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WarningsAllergy alert: do not use if you are allergic to omeprazole. omeprazole may cause severe skin reactions. Symptoms may include: skin reddening - blisters - rash - If an allergic reaction occurs, stop ...
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Directionsfor adults 18 years of age and older - this product is to be used once a day (every 24 hours), every day for 14 days - it may take 1 to 4 days for full effect; some people get complete relief of ...
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Other informationread the directions and warnings before use - keep the carton. It contains important information. store at 20-25°C (68-77°F) and protect from moisture
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Inactive ingredientsbenzyl alcohol, carmine, carnauba wax, FD&C blue #2/indigo carmine aluminum lake, flavor, hypromellose, hypromellose acetate succinate, lactose monohydrate, menthol, modified starch ...
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Questions or comments?1-888-423-0139
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Package/Label Principal Display PanelTopCare - ®health - COMPARE TO PRILOSEC OTC - ® Omeprazole - DELAYED RELEASE TABLETS 20 mg - ACID REDUCER - 24 HR - Treats Frequent Heartburn! WILDBERRY MINT COATED TABLET - SWALLOW – DO NOT ...
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INGREDIENTS AND APPEARANCEProduct Information