Label: CAREONE OMEPRAZOLE- omeprazole tablet, delayed release
- NDC Code(s): 72476-473-01, 72476-473-03
- Packager: Retail Business Services, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated April 17, 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) and protect from moisture
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Inactive ingredients carnauba wax, FD&C blue #1/brilliant blue FCF aluminum lake, hypromellose, hypromellose acetate succinate, lactose monohydrate, menthol, monoethanolamine, sodium lauryl sulfate, sodium starch ...
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Questions or comments? 1-800-719-9260
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Package/Label Principal Display Panel CAREone™ Compare to Prilosec OTC® OMEPRAZOLE - Delayed Release Tablets 20 mg - Acid Reducer - Treats Frequent Heartburn! OUR PHARMACISTS RECOMMEND - 42 TABLETS - Three 14-day courses of treatment - May take ...
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INGREDIENTS AND APPEARANCEProduct Information
