Other
Drug Facts
Safety Feature - Do not use if tablet blister unit is open or torn.
Dist. by Procter & Gamble,
Cincinnati, OH 45202
The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Prilosec Otc (NDC 84126-300). 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 other, active ingredient (in each tablet), purpose, use, warnings, otc - do not use, ask a doctor before use if you have:, ask a doctor or pharmacist before use if you are, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Safety Feature - Do not use if tablet blister unit is open or torn.
Dist. by Procter & Gamble,
Cincinnati, OH 45202
Omeprazole delayed-release tablet 20 mg (equivalent to 20.6 mg omeprazole magnesium)
Acid reducer
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.
Do not use if you have:
These may be signs of a serious condition. See your doctor.
taking a prescription drug.
Acid reducers may interact with certain prescription drugs.
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.
acetyl tributyl citrate, colloidal silicon dioxide, corn starch, croscarmellose sodium, hydroxypropyl cellulose, hypromellose 2910, magnesium stearate, methacrylic acid copolymer type c, microcrystalline cellulose, polyethylene glycol 400, polyethylene glycol 3350, polyethylene glycol 8000, polyvinyl alcohol, red iron oxide, sucrose, talc, titanium dioxide, triethyl citrate
1-800-289-9181
* Please review the disclaimer below.