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Pill Identifier Information of APAP 500 MG Oral Capsule

Drug Information

APAP 500 MG Oral Capsule

Imprint: 44;519
Shape: C48336
Color: C48326
Ingredients: Acetaminophen
Size: 19.00
Score: 1
Rxtty: SY
Author: WALGREEN CO.
Inactive Ingredients: CROSCARMELLOSE SODIUM / D&C RED NO. 33 / FD&C BLUE NO. 1 / FD&C RED NO. 40 / GELATIN / HYDROXYPROPYL CELLULOSE (TYPE H) / HYPROMELLOSES / FERROSOFERRIC OXIDE / FERRIC OXIDE YELLOW / POLYETHYLENE GLYCOLS / POVIDONES / PROPYLENE GLYCOL / STEARIC ACID / TITANIUM DIOXIDE>

Complete Information

  • Active ingredient (in each gelcap)

    Acetaminophen 500 mg

  • Purpose

    Pain reliever/fever reducer

  • Uses

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

    • blisters
    • rash
    • skin reddening

    • 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.

    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
    • any new symptoms appear
    • pain gets worse or lasts more than 10 days
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • Directions

  • children under 12 years: ask a doctor
  • Other information

  • 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

  • Questions or comments?

    1-800-426-9391 8:30 AM-4:00 PM ET, Monday-Friday

  • Principal Display Panel

    Walgreens

    Compare to the active ingredient in Extra
    Strength Tylenol® Rapid Release Gels††

    Pain
    Reliever
    ACETAMINOPHEN     500 mg /
    PAIN RELIEVER / FEVER REDUCER

    Extra Strength

    150 GELCAPS

    ACTUAL SIZE

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

    Walgreens Pharmacist Recommended.
    Our pharmacists recommend the
    Walgreens brand. We invite you to
    compare to national brands.
    ††This product is not manufactured or
    distributed by Kenvue Inc., owner of the
    registered trademark Extra Strength
    Tylenol® Rapid Release Gels.

    DISTRIBUTED BY: WALGREEN CO.
    DEERFIELD, IL 60015
    100% SATISFACTION GUARANTEED
    walgreens.com     ©2025 Walgreen Co.

    NDC 0363-0519-92

    50844    REV0525A51929
    REV-0825

    Walgreens 44-519

    Walgreens 44-519

  • INGREDIENTS AND APPEARANCE
    PAIN RELIEVER  EXTRA STRENGTH
    acetaminophen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0519
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    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 RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorred, blueScoreno score
    ShapeOVALSize19mm
    FlavorImprint Code L;5
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0519-081 in 1 CARTON05/10/2004
    124 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:0363-0519-151 in 1 CARTON05/10/2004
    250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3NDC:0363-0519-121 in 1 CARTON05/10/2004
    3100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4NDC:0363-0519-92150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/10/2004
    5NDC:0363-0519-371 in 1 CARTON12/30/2024
    575 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    6NDC:0363-0519-191 in 1 CARTON05/10/200410/05/2018
    68 in 1 VIAL; Type 0: Not a Combination Product
    7NDC:0363-0519-201 in 1 CARTON05/10/200404/13/2024
    7225 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    8NDC:0363-0519-29150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/10/200407/07/2024
    9NDC:0363-0519-54375 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/10/200405/19/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01305/10/2004
    Labeler - Walgreen Company (008965063)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.038154464manufacture(0363-0519) , pack(0363-0519)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867837manufacture(0363-0519)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867894manufacture(0363-0519)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.868734088manufacture(0363-0519)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.967626305pack(0363-0519)