Active Ingredient (In Each Capsule)
Esomeprazole 20 mg
(Each delayed-release capsule corresponds to 22 mg esomeprazole magnesium dihydrate)
The following Structured Product Label (SPL) was submitted to the FDA by Meijer Distribution Inc for the product Esomeprazole Magnesium (NDC 41250-727). 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 capsule), purpose, uses, 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.
Esomeprazole 20 mg
(Each delayed-release capsule corresponds to 22 mg esomeprazole magnesium dihydrate)
Acid reducer
Allergy alert: Do not use if you are allergic to esomeprazole
These may be signs of a serious condition. See your doctor.
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 Courses (if needed)
FD&C blue no. 1, FD&C blue no. 1 aluminum lake, FD&C red no. 3, ferric oxide, gelatin, glyceryl monostearate, hypromellose, magnesium stearate, meglumine, methacrylic acid and ethyl acrylate copolymer dispersion, polyethylene glycol, polysorbate 80, shellac, sodium lauryl sulfate, sugar spheres, talc, titanium dioxide, triethyl citrate
1-800-719-9260
Compare to Nexium® 24 HR Clear Minis™ active ingredient
24 HOUR
esomeprazole magnesium
Delayed-Release Capsules, 20 mg Acid Reducer
SEE NEW WARNING INFORMATION
MINI CAPSULES
Treats Frequent Heartburn
14 Capsules
one 14-day course of treatment may take 1 to 4 days for full effect
actual size
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