Label: OMEPRAZOLE, 24/7 LIFE BY 7-ELEVEN- omeprazole tablet, delayed release tablet, delayed release

  • NDC Code(s): 66715-6550-4
  • Packager: Lil' Drug Store Products, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 5, 2025

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  • Drug Facts

  • Active ingredient

    ​Active ingredient (in each tablet)

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

    Purpose

    Purpose

    Acid redcer

  • Use

    Use

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

    Allergy Alert

    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

    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 shoulder pain 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

    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

    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

    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

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    Directions

    ■ 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 crush or chew 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.

  • Other information

    Other information

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

    Inactive ingredients

    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

  • Questions or comments

    Questions or comments?

    Call toll free 1-877-507-6516 (M-F 8AM-4:30PM CST)

  • Tips for Managing Heartburn

    Tips for Managing Heartburn

    • Do not lie flat or bend over after eating
    • Do not wear tight-fitting clothing around the stomach
    • Do not eat before bedtime
    • Raise the head of your bed
    • Avoid heartburn-causing foods such as rich, spicy, fatty or fried foods, chocolate, caffeine, alcohol and certain fruits and vegetables
    • Eat slowly and avoid big meals
    • If overweight, lose weight
    • Quit smoking
  • Omeprazole, 24/7 Life by 7-Eleven

    24/7 Life by 7-Eleven TM

    See current Drug Facts

    Omeprazole
    Delayed-Release
    Tablets 20 mg
    Acid Reducer 24HR
    Treats Frequent Heartburn!
    May take 1 to 4 days for full effect

    †compare to
    PRILOSEC OTC ®
    active ingredient

    14

    TABLETS

    One 14-day course of treatment

    [tablet image]

    Actual Size

    PDP/Package

  • INGREDIENTS AND APPEARANCE
    OMEPRAZOLE, 24/7 LIFE BY 7-ELEVEN 
    omeprazole tablet, delayed release tablet, delayed release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6550
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OMEPRAZOLE MAGNESIUM (UNII: 426QFE7XLK) (OMEPRAZOLE - UNII:KG60484QX9) OMEPRAZOLE20.6 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACETYL TRIBUTYL CITRATE (UNII: 0ZBX0N59RZ)  
    POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)  
    SUCROSE (UNII: C151H8M554)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER (UNII: NX76LV5T8J)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    TALC (UNII: 7SEV7J4R1U)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    Product Characteristics
    Colorred ((reddish brown)) Scoreno score
    ShapeOVALSize13mm
    FlavorImprint Code O
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-6550-41 in 1 CARTON06/15/2025
    114 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00106/09/2025
    Labeler - Lil' Drug Store Products, Inc. (093103646)
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