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. The maximum daily dose of this product is 6 gelcaps (3,000 mg) in 24 hours. 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

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

  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

  • store at 25ºC (77ºF); excursions permitted between 15°-30°C (59°-86°F)
  • avoid high humidity
  • see end flap for expiration date and lot number

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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 or comments?

  1-888-309-9030

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• Principal Display Panel

  DGâ„¢|health

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

  Extra Strength
  Pain Relief
  Acetaminophen 500 mg
  Pain Reliever/Fever Reducer
  Contains no aspirin

  500
  mg each    

  Rapid Release

  100 Gelcaps

  Actual Gelcap Size

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

  *This product is not manufactured or distributed by McNeil Consumer
  Healthcare, owner of the registered trademark Extra Strength Tylenol®
  Rapid Release Gels.
  50844   REV0615H51912

  DISTRIBUTED BY
  DOLGENCORP, LLC
  100 MISSION RIDGE
  GOODLETTSVILLE, TN 37072

  100%
  Satisfaction
  Guaranteed!
  (888) 309-9030

  

  Dollar General 44-519

  
  

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• INGREDIENTS AND APPEARANCE

  PAIN RELIEF  EXTRA STRENGTH acetaminophen tablet

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-519 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 (UNII: 2G86QN327L)   HYPROMELLOSES (UNII: 3NXW29V3WO)   FERROSOFERRIC OXIDE (UNII: XM0M87F357)   FERRIC OXIDE YELLOW (UNII: EX438O2MRT)   POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)   POVIDONE (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:55910-519-12 1 in 1 CARTON 05/10/2004 07/19/2020 1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:55910-519-15 1 in 1 CARTON 05/10/2004 07/19/2020 2 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part343 05/10/2004 07/19/2020

  Labeler - DOLGENCORP, LLC (068331990)

  Establishment
  Name	Address	ID/FEI	Business Operations
  LNK International, Inc.		038154464	PACK(55910-519)

  Establishment
  Name	Address	ID/FEI	Business Operations
  LNK International, Inc.		832867837	MANUFACTURE(55910-519) , PACK(55910-519)

  Establishment
  Name	Address	ID/FEI	Business Operations
  LNK International, Inc.		967626305	PACK(55910-519)

  Establishment
  Name	Address	ID/FEI	Business Operations
  LNK International, Inc.		868734088	PACK(55910-519)

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