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Rapid Release Pain Reliever (Target Corporation)

Available Formats

Dosage Form Package Information Links
CAPSULE, LIQUID FILLED 1 BOTTLE in 1 CARTON (11673-519-12) > 100 CAPSULE, LIQUID FILLED in 1 BOTTLE Label Information
CAPSULE, LIQUID FILLED 1 BOTTLE, PLASTIC in 1 CARTON (11673-519-15) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC Label Information
CAPSULE, LIQUID FILLED 1 BOTTLE, PLASTIC in 1 CARTON (11673-519-20) > 225 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC Label Information

Complete Rapid Release Pain Reliever Information

  • Active ingredient (in each gelcap)

    Acetaminophen 500 mg


  • Purpose

    Pain reliever/fever reducer


  • Uses

    • temporarily relieves minor aches and pains due to:
      • headache
      • the common cold
      • muscular aches
      • backache
      • minor pain of arthritis  
      • toothache
      • premenstrual and menstrual cramps
    • temporarily reduces fever

  • Warnings

    Liver warning:  This product contains acetaminophen. Severe liver damage may occur if you take:

    • more than 4,000 mg of acetaminophen in 24 hours
    • with other drugs containing acetaminophen
    • 3 or more alcoholic drinks every day while using this product

    Allergy alert:  Acetaminophen may cause severe skin reactions. Symptoms may include:

    • skin reddening
    • blisters
    • rash

    If a skin reaction occurs, stop use and seek medical help right away.

    Do not use
    • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    • if you are allergic to acetaminophen or any of the inactive ingredients in this product 

    Ask a doctor before use if you have

    liver disease.

    Ask a doctor or pharmacist before use if you are

    taking the blood thinning drug warfarin.

    Stop use and ask a doctor if
    • pain gets worse or lasts more than 10 days
    • fever gets worse or lasts more than 3 days
    • new symptoms occur
    • redness or swelling is present

    These could be signs of a serious condition.

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    In case of accidental overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms. 


  • Directions

    • do not take more than directed
    • adults and children 12 years and over
      • take 2 gelcaps every 6 hours while symptoms last
      • do not take more than 6 gelcaps in 24 hours, unless directed by a doctor
      • do not take for more than 10 days unless directed by a doctor
    • children under 12 years: ask a doctor

  • Other information

    • avoid high humidity 
    • store at 25ºC (77ºF); excursions permitted between 15°-30°C (59°-86°F)
    • use by expiration date on package

  • Inactive ingredients

    croscarmellose sodium, D&C red #33, FD&C blue #1, FD&C red #40, gelatin, hydroxypropyl cellulose, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, stearic acid, titanium dioxide


  • Questions?

    Call 1-800-910-6874


  • Principal Display Panel 

    NDC 11673-519-20

    Compare to active ingredient in
    Extra Strength Tylenol® Rapid Release Gels*

    extra strength
    acetaminophen
    gelcaps, 
    500 mg

    pain reliever/fever reducer
    quick release

    up&up®

    225 GELCAPS

    225
    GELCAPS

    TAMPER EVIDENT: DO NOT USE IF IMPRINTED
    SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

    *This product is not manufactured or distributed
    byJohnson & Johnson Corporation, owner of the
    registered trademark Extra Strength Tylenol®
    Rapid Release Gels.    50844     REV0417B51920

    094 01 0309 R04 ID225450
    Distributed by Target Corporation
    Minneapolis, MN 55403
    ©2017 Target Brands, Inc.
    Shop Target.com

    Target 44-519

    Target 44-519


  • INGREDIENTS AND APPEARANCE
    ACETAMINOPHEN  EXTRA STRENGTH
    acetaminophen tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-519
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg
    Inactive Ingredients
    Ingredient Name Strength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    SHELLAC (UNII: 46N107B71O)  
    Product Characteristics
    Color RED, BLUE Score no score
    Shape OVAL Size 19mm
    Flavor Imprint Code L;5
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-519-12 100 in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2004
    2 NDC:11673-519-15 50 in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2004
    3 NDC:11673-519-20 225 in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2004
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part343 05/10/2004
    Labeler - Target Corporation (006961700)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867837 MANUFACTURE(11673-519) , PACK(11673-519)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 038154464 PACK(11673-519)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 967626305 PACK(11673-519)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 868734088 PACK(11673-519)