Active Ingredient (In Each Tablet)
Omeprazole USP 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by The Kroger Company for the product Omeprazole (NDC 30142-992). 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, uses, warnings, directions, other information, inactive ingredients, questions or comments, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Omeprazole USP 20 mg
Acid reducer
Allergy alert: Do not use if you are allergic to omeprazole.
Do not use if you have:
These may be signs of a serious condition. See your doctor.
Ask a doctor before use if you have:
Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.
Stop use and ask a doctor if:
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. 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)
anhydrous lactose, hypromellose, hypromellose acetate succinate, iron oxide red, iron oxide yellow, lactose monohydrate, methyl cellulose, monoethanolamine, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, sodium stearate, sodium stearyl fumarate, talc, triethyl citrate and titanium dioxide.
The imprinting ink contains ammonium hydroxide, black iron oxide, n-butyl alcohol, propylene glycol and shellac.
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