Label: DG HEALTH OMPERAZOLE- omeprazole tablet, orally disintegrating, delayed release

  • NDC Code(s): 55910-713-30, 55910-713-55, 55910-713-74
  • Packager: Dolgencorp Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated January 31, 2025

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  • Active ingredient (in each tablet)
    Omeprazole 20 mg
  • Purpose
    Acid reducer
  • Use
    • treats frequent heartburn (occurs 2 or more days 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 ...
  • 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 ...
  • Other information
    • read the directions and warnings before use - • keep the carton. It contains important information. • store at 20-25°C (68-77°F); keep product out of high heat and moisture - • take the tablet ...
  • Inactive ingredients
    amino methacrylate copolymer, ascorbic acid, cetyl alcohol, colloidal silicon dioxide, crospovidone, ferric oxide, flavor, hypromellose, hypromellose phthalate, maize maltodextrin, mannitol ...
  • Questions or comments?
    1-800-719-9260: weekdays 7:30 AM to 5:00 PM EST
  • Package/Label Principal Display Panel
    DG™|health - Compare to Prilosec OTC® MELTech® Melts In Your Mouth - Omeprazole - Delayed Release Orally Disintegrating Tablets, 20 mg - Acid Reducer - Treats Frequent Heartburn! 24 HR - DISSOLVE ...
  • INGREDIENTS AND APPEARANCE
    Product Information