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 Cardinal Health 110, Llc. Dba Leader for the product Leader Esomeprazole Magnesium (NDC 70000-0727). 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:
If an allergic reaction occurs, stop use and seek medical help right away.
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 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
LEADERTM
24 Hour Capsules
Esomeprazole Magnesium
Delayed-Release Capsules, 20 mg Acid Reducer
Treats Frequent Heartburn
May Take 1 to 4 Days for Full Effect
COMPARE TO NEXIUM® 24HR active ingredient
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Actual Size
14 CAPSULES
One 14-Day Course of Treatment
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