Label: TYLENOL 8 HR ARTHRITIS PAIN- acetaminophen tablet, extended release

  • NDC Code(s): 50580-783-10, 50580-783-24, 50580-783-25, 50580-783-29, view more
    50580-783-30, 50580-783-32
  • Packager: Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated November 19, 2020

If you are a consumer or patient please visit this version.


    Drug Facts

  • Active ingredient (in each caplet)

    Acetaminophen 650 mg

  • Purpose

    Pain reliever/fever reducer

  • Uses

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

    Liver warning

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

    • more than 6 caplets in 24 hours, which is the maximum daily amount
    • 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.

    Overdose warning

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

  • Directions

    • take 2 caplets every 8 hours with water
    • swallow whole; do not crush, chew, split or dissolve
    • do not take more than 6 caplets in 24 hours
    • do not use for more than 10 days unless directed by a doctor
    under 18 years of age
    • ask a doctor
  • Other information

    • store between 20-25°C (68-77°F)
    • do not use if carton is opened. Do not use if foil inner seal imprinted with "TYLENOL" is broken or missing
  • Inactive ingredients

    carnauba wax, hydroxyethyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, modified starch, povidone, powdered cellulose, pregelatinized starch, sodium starch glycolate, titanium dioxide, triacetin

  • Questions or comments?

    call 1-877-895-3665 (toll-free) or 215-273-8755 (collect)


    NDC 50580-783-32



    Extended-release tablets

    Pain Reliever / Fever Reducer

    For The Temporary Relief
    Of Minor Arthritis Pain

    Bi-Layer Tablets

    Actual Size

    100 Caplets*
    650 mg each

    Principal Display Panel
    acetaminophen tablet, extended release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50580-783
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen650 mg
    Inactive Ingredients
    Ingredient NameStrength
    carnauba wax (UNII: R12CBM0EIZ)  
    hydroxyethyl cellulose (140 mpa.s at 5%) (UNII: 8136Y38GY5)  
    hypromellose, unspecified (UNII: 3NXW29V3WO)  
    magnesium stearate (UNII: 70097M6I30)  
    microcrystalline cellulose (UNII: OP1R32D61U)  
    povidone, unspecified (UNII: FZ989GH94E)  
    powdered cellulose (UNII: SMD1X3XO9M)  
    sodium starch glycolate type a potato (UNII: 5856J3G2A2)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    triacetin (UNII: XHX3C3X673)  
    Product Characteristics
    ColorWHITEScoreno score
    FlavorImprint Code TYLENOL;ER
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50580-783-101 in 1 CARTON07/13/2015
    1100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:50580-783-241 in 1 CARTON07/13/2015
    224 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3NDC:50580-783-251 in 1 CARTON07/13/2015
    3225 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4NDC:50580-783-291 in 1 CARTON07/13/201511/30/2020
    4290 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    5NDC:50580-783-30290 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2018
    6NDC:50580-783-321 in 1 CARTON08/26/2019
    6100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Labeler - Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division (878046358)