Available Formats

• Active ingredient (in each gelcap)

  Acetaminophen 500 mg

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• Purpose

  Pain reliever/fever reducer

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• 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

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• 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. 

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• 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

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• Other information

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

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• 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

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• Questions?

  Call 1-800-910-6874

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• 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

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• 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)

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