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Pill Identifier Information of APAP 500 MG Oral Tablet

Drug Information

APAP 500 MG Oral Tablet

Imprint: 44;175
Shape: C48336
Color: C48325
Ingredients: Acetaminophen
Size: 18.00
Score: 1
Rxtty: SY
Author: L.N.K. International, Inc.
Inactive Ingredients: HYPROMELLOSES / POVIDONES / STEARIC ACID / CASTOR OIL / SODIUM STARCH GLYCOLATE TYPE A POTATO>

Complete Information

  • Active ingredient (in each caplet)

    Acetaminophen 500 mg

  • Purpose

    Pain reliever/fever reducer

  • Uses

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

    • 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.

    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
    • any new symptoms appear
    • 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

    castor oil, hypromellose, povidone, sodium starch glycolate, starch, stearic acid

  • Questions or comments?

    1-800-426-9391

  • Principal Display Panel

    QUALITY
    +PLUS

    NDC 50844-175-12

    *Compare to active ingredient in
    Extra Strength Tylenol® Caplets

    EXTRA STRENGTH
    PAIN RELIEVER
    Acetaminophen 500 mg
    PAIN RELIEVER/FEVER REDUCER

    ACTUAL
    SIZE

    100 Caplets

    CONTAINS NO ASPIRIN

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

    *This product is not manufactured or distributed by Kenvue Inc.,
    owner of the registered trademark Extra Strength Tylenol®
    Caplets.       50844            ORG102417512

    Distributed by
    LNK INTERNATIONAL, INC.
    60 Arkay Drive
    Hauppauge, NY 11788
    USA

    Quality plus 44-175

    Quality plus 44-175

  • INGREDIENTS AND APPEARANCE
    PAIN RELIEVER  EXTRA STRENGTH
    acetaminophen tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50844-175
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    CASTOR OIL (UNII: D5340Y2I9G)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeOVALSize17mm
    FlavorImprint Code 44;175
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50844-175-121 in 1 CARTON04/02/1993
    1100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:50844-175-94100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/02/199309/30/2023
    3NDC:50844-175-081 in 1 CARTON04/02/199304/19/2022
    324 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4NDC:50844-175-101 in 1 CARTON04/02/199304/19/2022
    440 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01304/02/1993
    Labeler - L.N.K. International, Inc. (038154464)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.038154464pack(50844-175)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867837manufacture(50844-175)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867894manufacture(50844-175)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.868734088manufacture(50844-175)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.967626305pack(50844-175)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.117597853pack(50844-175)