Active Ingredients (In Each Capsule)
Omeprazole 20 mg
Sodium Bicarbonate 1100 mg
The following Structured Product Label (SPL) was submitted to the FDA by Riley Consumer Care, Llc for the product Zegerid Otc (NDC 82632-101). 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 ingredients (in each capsule), 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 taking a prescription drug., 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
Sodium Bicarbonate 1100 mg
Acid reducer
Allows absorption of this omeprazole product
Allergy alert:
• do not use if you are allergic to omeprazole.
• omeprazole may cause severe skin reactions.
Symptoms may include:
• skin reddening
• blisters
• rash
If an allergic reaction occurs, stop use and seek medical help right away.
These may be signs of a serious condition. See your doctor.
Acid reducers may interact with certain prescription drugs.
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).
citric acid anhydrous, croscarmellose sodium, FD&C blue #1 aluminum lake, gelatin, magnesium stearate, polysorbate 80, potassium sorbate, propylene glycol, shellac, sodium lauryl sulphate and titanium dioxide.
Call 1-888-4-ZEG-OTC (1-888-493-4682) between 9:00 AM and 5:00 PM Eastern Standard Time, Monday through Friday
CLINICALLY PROVEN TO
Treat Frequent Heartburn
Zegerid
OTC®
• Omeprazole 20 mg/Acid Reducer
• Sodium Bicarbonate 1100 mg
/Allows Absorption of this
Omeprazole Product
24 HOUR
14
CAPSULES
One 14-Day Course of Treatment
MAY TAKE 1 TO 4 DAYS FOR FULL EFFECT
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