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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- Official Label (Printer Friendly)
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Active ingredient (in each tablet) Omeprazole 20 mg
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Purpose Acid reducer
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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
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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 ...
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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 ...
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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 ...
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Inactive ingredients amino methacrylate copolymer, ascorbic acid, cetyl alcohol, colloidal silicon dioxide, crospovidone, ferric oxide, flavor, hypromellose, hypromellose phthalate, maize maltodextrin, mannitol ...
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Questions or comments? 1-800-719-9260: weekdays 7:30 AM to 5:00 PM EST
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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 ...
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INGREDIENTS AND APPEARANCEProduct Information