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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  • Active ingredient (in each tablet)
    Omeprazole 20 mg
  • Purpose
    Acid reducer
  • Use
    treats 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
  • Warnings
    Allergy 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 ...
  • Directions
    for 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 ...
  • Other information
    read 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
  • Inactive ingredients
    benzyl alcohol, carmine, carnauba wax, FD&C blue #2/indigo carmine aluminum lake, flavor, hypromellose, hypromellose acetate succinate, lactose monohydrate, menthol, modified starch ...
  • Questions or comments?
    1-888-423-0139
  • Package/Label Principal Display Panel
    TopCare - ®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 ...
  • INGREDIENTS AND APPEARANCE
    Product Information