Other
Drug Facts
Dist. by Procter & Gamble,
Cincinnati, OH 45202
Product of Sweden
The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Prilosec Otc (NDC 37000-459). 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, allergy alert, otc - do not use, ask a doctor before use if you have, otc - ask doctor/pharmacist, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Dist. by Procter & Gamble,
Cincinnati, OH 45202
Product of Sweden
Omeprazole delayed-release tablet 20 mg (equivalent to 20.6 mg omeprazole magnesium)
Acid reducer
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 or pharmacist before use if you are taking
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.
FD&C blue no. 2 aluminum lake, FD&C red no. 40 aluminum lake, flavor, glyceryl monostearate, hydroxypropyl cellulose, hypromellose, magnesium stearate, methacrylic acid copolymer, mica, microcrystalline cellulose, polyethylene glycol 6000, polysorbate 80, polyvinylpyrrolidone, saccharin sodium, sodium stearyl fumarate, starch, sucrose, talc, titanium dioxide, triethyl citrate
1-800-289-9181
Treats FREQUENT Heartburn!
Occurring 2 Or More Days A Week
NDC 37000-459-02
Prilosec OTC ®
omeprazole delayed-release tablets
20 mg / acid reducer
SWALLOW - DO NOT CHEW
14 TABLETS
One 14-day course of treatment
Coated with
Wildberry Flavor
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