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Prilosec OTC Prescribing Information

Package insert / product label
Generic name: omeprazole magnesium
Dosage form: tablet, delayed release
Drug class: Proton pump inhibitors

Medically reviewed by Drugs.com. Last updated on Jul 15, 2024.

Drug Facts

Active ingredient (in each tablet)

Omeprazole delayed-release tablet 20 mg (equivalent to 20.6 mg omeprazole magnesium)

Purpose

Acid reducer

Indications and Usage for Prilosec OTC

  • treats frequent heartburn (occurs 2 or moredays a week)
  • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Warnings

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:

  • trouble or pain swallowing food, vomiting with blood, or bloody or black stools
  • heartburn with lightheadedness, sweating or dizziness
  • chest pain or shoulderpain with shortness of breath; sweating; pain spreading to arms, neck, or shoulders; or lightheadedness
  • frequent chest pain

These may be signs of a serious condition. See your doctor.

Ask a doctor before use if you have:

  • had heartburn over 3 months. This may be a sign of a more serious condition.
  • frequent wheezing, particularly with heartburn
  • unexplained weight loss
  • nausea or vomiting
  • stomach pain

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:

• your heartburn continues or worsens
• you need to take this product for more than 14 days
• you need to take more than 1 course of treatment every 4 months
• you get diarrhea

• you develop a rash or joint pain

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.

Prilosec OTC Dosage and Administration

  • for adults 18 years of age and older
  • this product is to be used once a day (every 24 hours), every day for 14 days
  • it may take 1 to 4 days for full effect; some people get complete relief of symptoms within 24 hours

    14-Day Course of Treatment
    • swallow 1 tablet with a glass of water before eating in the morning
    • take every day for 14 days
    • do not take more than 1 tablet a day
    • do not use for more than 14 days unless directed by your doctor
    • swallow whole. Do not chew, crush, or suck tablets.
    Repeated 14-Day Courses (if needed)
    • you may repeat a 14-day course every 4 months
    • do not take for more than 14 days or more often than every 4 months unless directed by a doctor
  • children under 18 years of age: ask a doctor. Heartburn in children may sometimes be caused by a serious condition.

Storage and Handling

  • read the directions and warnings before use
  • keep the carton. It contains important information.
  • store at 20-25°C (68-77°F) and protect from moisture

Inactive ingredients

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

Questions?

1-800-289-9181

Safety Feature - Do not use if tablet blister unit is open or torn.

Dist. by Procter & Gamble,
Cincinnati, OH 45202

Product of Sweden

PRINCIPAL DISPLAY PANEL - 14 Tablet Carton

See current Drug Facts NDC 37000-459-02

Treats FREQUENT Heartburn! 24 HR

Prilosec OTC ®


omeprazole delayed-release tablets

20 mg / acid reducer

SWALLOW - DO NOT CHEW

14 TABLETS

One 14-day course of treatment

May take 1 to 4 days for full effect

WILDBERRY Coated Tablet

459

PRILOSEC OTC
omeprazole magnesium tablet, delayed release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-459
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OMEPRAZOLE MAGNESIUM (UNII: 426QFE7XLK) (OMEPRAZOLE - UNII:KG60484QX9) OMEPRAZOLE20 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, RICE (UNII: 4DGK8B7I3S)
POVIDONE K60 (UNII: SZR7Z3Q2YH)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
FD&C BLUE NO. 2--ALUMINUM LAKE (UNII: 4AQJ3LG584)
FD&C RED NO. 40 (UNII: WZB9127XOA)
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICA (UNII: V8A1AW0880)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
Product Characteristics
ColorpurpleScoreno score
ShapeOVALSize15mm
FlavorBERRYImprint CodeP
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-459-011 in 1 POUCH; Type 0: Not a Combination Product08/15/2012
2NDC:37000-459-0214 in 1 CARTON08/15/2012
21 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:37000-459-032 in 1 CARTON08/15/201212/01/2022
314 in 1 CARTON
31 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:37000-459-043 in 1 CARTON08/15/2012
414 in 1 CARTON
41 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:37000-459-051 in 1 BLISTER PACK; Type 0: Not a Combination Product08/15/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02122908/15/2012
Labeler - The Procter & Gamble Manufacturing Company (004238200)
Registrant - AstraZeneca AB (Sweden) (876516568)

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