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Pill Identifier Information of Tylenol 500 MG Oral Tablet

Drug Information

Tylenol 500 MG Oral Tablet

Imprint: TYLENOL;500;HOSPITAL
Shape: C48345
Color: C48325
Ingredients: Acetaminophen
Size: 18.00
Score: 1
Rxtty: SY
Author: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Inactive Ingredients: Carnauba wax / castor oil / starch, corn / FD&C red No. 40 / aluminum oxide / hypromelloses / magnesium stearate / Polyethylene glycols / powdered cellulose / propylene glycol / shellac / Sodium Starch Glycolate Type A Potato / titanium dioxide>

Complete Information

  • 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

    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

    adults and children 12 years and over
    • take 2 caplets every 6 hours while symptoms last
    • do not take more than 6 caplets in 24 hours, unless directed by a doctor
    • do not use for more than 10 days unless directed by a doctor
    children under 12 yearsask a doctor
  • Other information

  • Inactive ingredients

    carnauba wax 1, castor oil 1, corn starch, FD&C red no. 40 aluminum lake, hypromellose, magnesium stearate, polyethylene glycol 1, powdered cellulose, pregelatinized starch, propylene glycol, shellac, sodium starch glycolate, titanium dioxide

    1
    contains one or more of these ingredients
  • Questions or comments?

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

  • PRINCIPAL DISPLAY PANEL

    NDC 50580-451-50

    See New Warnings Information & Directions

    TYLENOL ®

    Pain Reliever
    Fever Reducer
    Acetaminophen

    EXTRA
    STRENGTH
    For Adults

    50 CAPLETS
    500 mg each

    Caplets

    For Hospital and Government Use Only

    Principal Display Panel
  • INGREDIENTS AND APPEARANCE
    TYLENOL  EXTRA STRENGTH
    acetaminophen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50580-451
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeOVALSize18mm
    FlavorImprint Code TYLENOL;500;HOSPITAL
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50580-451-03150 in 1 CARTON08/19/199411/30/2016
    11 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:50580-451-1010 in 1 CARTON06/30/201401/31/2019
    210 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:50580-451-501 in 1 CARTON08/19/1994
    350 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4NDC:50580-451-70700 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/19/1994
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01308/19/1994
    Labeler - Kenvue Brands LLC (118772437)