Active Ingredient (In Each Tablet)
Omeprazole 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by American Sales Company for the product Careone Omeprazole (NDC 41520-939). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, use, warnings, do not use if you have:, ask a doctor before use if you have:, ask a doctor or pharmacist before use if you are, stop use and ask a doctor if:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Omeprazole 20 mg
Acid reducer
Allergy alert: do not use if you are allergic to omeprazole
These may be signs of a serious condition. See your doctor.
taking:
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
14-Day Course of Treatment
Repeated 14-Day Course (if needed)
amino methacrylate copolymer, ascorbic acid, cetyl alcohol, colloidal silicon dioxide, crospovidone, ferric oxide, flavor, hypromellose, hypromellose phthalate, maize maltodextrin, mannitol, microcrystalline cellulose, propylene glycol, silicon dioxide, sodium stearate, sodium stearyl fumarate, sorbitol, sucralose, sugar spheres, talc, titanium dioxide, triethyl citrate
1-800-719-9260: weekdays 7:30 AM to 5:00 PM EST
OMEPRAZOLE
Delayed Release Orally Disintegrating Tablets 20mg
Acid Reducer
Treats Frequent Heartburn!
Occurring 2 or More Days a Week
Orally Disintegrating Tablets
Melts in your mouth
Actual Size ● Strawberry Flavor
14 TABLETS
One 14-day course of treatment
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