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Pill Identifier Information of Tylenol 500 MG Oral Tablet

Drug Information

Tylenol 500 MG Oral Tablet

Imprint: TYLENOL;500
Shape: C48345
Color: C48325
Ingredients: Acetaminophen
Size: 18.00
Score: 1
Rxtty: SY
Author: Lil' Drug Store Products, 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 / 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

    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

    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, corn starch 1, FD&C red no. 40 aluminum lake, hypromellose, magnesium stearate, modified starch 1, 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)

  • SPL UNCLASSIFIED SECTION

    Product distributed by:
    JOHNSON & JOHNSON CONSUMER INC.
    McNeil Consumer Healthcare Division
    Fort Washington, PA 19034 USA

  • SPL UNCLASSIFIED SECTION

    Repackaged and distributed by:
    Lil' Drug Store Products, Inc., 9300 Earhart Lane SW
    Cedar Rapids, IA 52404

  • Tylenol ES Caplets, Lil' Drug Store ® - PDP/Package

    TYLENOL ®

    FOR ADULTS

    Acetaminophen

    Pain Reliever

    Fever Reducer

    EXTRA STRENGTH

    500 mg each

    6

    Caplets

    Lil'

    Drug Store ®

    Principal Display Panel - 500 mg Caplet Pouch Carton

  • Tylenol ES Caplets, TRAVEL BASIX - PDP/Package

    TYLENOL ®

    FOR ADULTS

    Acetaminophen Pain Reliever Fever Reducer

    Extra Strength

    [caplets image]

    500 mg each

    4

    Caplets

    2 POUCHES OF 2 CAPLETS EACH

    [TRAVEL BASIX logo]

    PDP/Package

  • Tylenol ES Caplets, CVP ® HEALTH - PDP/Package

    TYLENOL ®

    FOR ADULTS

    Acetaminophen Pain Reliever Fever Reducer

    Extra Strength

    [caplets image]

    500 mg each

    4

    Caplets

    2 POUCHES OF 2 CAPLETS EACH

    [CVP ® HEALTH logo]

    PDP/Package

  • Tylenol ® ES Caplets, Lil' Drug Store ® 25ct Unit Dose Box - PDP/Package

    TYLENOL®

    FOR ADULTS

    Acetaminophen

    Pain Reliever

    Fever Reducer

    Extra Strength

    [caplets image]

    25 Pouches of 2 Caplets each - 500 mg each

    [Lil' Drug Store logo]

    PDP/Package

  • Tylenol ® ES Caplets, Lil' Drug ® Store 30ct Unit Dose Box - PDP/Package

    TYLENOL®

    FOR ADULTS

    Acetaminophen

    Pain Reliever

    Fever Reducer

    Extra Strength

    [caplets image]

    30 Pouches of 2 Caplets each - 500 mg each

    [Lil' Drug Store logo]

    PDP/Package

  • INGREDIENTS AND APPEARANCE
    TYLENOL EXTRA STRENGTH, TRAVEL BASIX 
    acetaminophen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6447
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeOVALSize18mm
    FlavorImprint Code TYLENOL;500
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-6447-22 in 1 CARTON11/29/2022
    12 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01311/22/2022
    TYLENOL EXTRA STRENGTH, CVP HEALTH 
    acetaminophen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6547
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeOVALSize18mm
    FlavorImprint Code TYLENOL;500
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-6547-22 in 1 CARTON05/06/2022
    12 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01305/06/2022
    TYLENOL EXTRA STRENGTH 
    acetaminophen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-9747
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeOVALSize18mm
    FlavorImprint Code TYLENOL;500
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-9747-11 in 1 CARTON04/16/201806/29/2024
    12 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:66715-9747-22 in 1 CARTON04/13/2019
    22 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:66715-9747-33 in 1 CARTON06/29/2018
    32 in 1 POUCH; Type 0: Not a Combination Product
    4NDC:66715-9747-730 in 1 CARTON04/09/2018
    42 in 1 POUCH; Type 0: Not a Combination Product
    5NDC:66715-9747-825 in 1 BOX, UNIT-DOSE04/19/202208/12/2028
    52 in 1 POUCH; Type 0: Not a Combination Product
    6NDC:66715-9747-930 in 1 BOX, UNIT-DOSE04/19/2022
    62 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01308/09/2011
    Labeler - Lil' Drug Store Products, Inc. (093103646)