Active Ingredient (In Each Capsule)
*Omeprazole delayed-release capsules 20 mg
(equivalent to 20.6 mg omeprazole magnesium)
The following Structured Product Label (SPL) was submitted to the FDA by Gericare Pharmaceuticals for the product Omeprazole Magnesium (NDC 57896-759). 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.
*Omeprazole delayed-release capsules 20 mg
(equivalent to 20.6 mg omeprazole magnesium)
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.
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
black iron oxide, dibasic calcium phosphate, gelatin, glyceryl monostearate, hypromellose 3 cps, magnesium oxide, magnesium stearate, methacrylic acid copolymer dispersion, methacrylic acid copolymer Type B, microcrystalline cellulose, polysorbate 80, potassium hydroxide, propylene glycol, red iron oxide, shellac, silicon dioxide, sodium lauryl sulfate, sugar spheres, talc, titanium dioxide, triethyl citrate
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GERICARE
Omeprazole
Delayed-Release Capsules
20 mg*
Compare to active ingredient in Prilosec OTC**
NDC 57896-759-42
Acid Reducer
Treats Frequent Heartburn!
Occurring 2 or more Days a Week
42 Capsules (Safety Sealed)
Three 14-Day Courses of treament
* Please review the disclaimer below.