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Pain Reliever (NASH-FINCH COMPANY)

Available Formats

Dosage Form Package Information Links
TABLET 1 BOTTLE, PLASTIC in 1 CARTON (70253-175-15) > 50 TABLET in 1 BOTTLE, PLASTIC Label Information
TABLET 1 BOTTLE, PLASTIC in 1 CARTON (70253-175-08) > 24 TABLET in 1 BOTTLE, PLASTIC Label Information
TABLET 1 BOTTLE, PLASTIC in 1 CARTON (70253-175-12) > 100 TABLET in 1 BOTTLE, PLASTIC Label Information
TABLET 500 TABLET in 1 BOTTLE, PLASTIC (70253-175-14) Label Information

Complete Pain Reliever Information

  • Active ingredients (in each tablet)

    Acetaminophen 500 mg


  • Purpose

    Pain reliever/fever reducer


  • Uses

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

  • Warnings

    Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 6 caplets (3,000 mg) in 24 hours. 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.

    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 of breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    Overdose warning: Taking more than the recommended dose (overdose) may cause liver damamge. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.


  • Directions

    • do not take more than directed
      (see overdose warning)
    • adults and children 12 years and over
      • take 2 caplets every 4 to 6 hours while symptoms last
      • do not take more than 8 caplets in 24 hours
      • do not take for more than 10 days unless directed by a doctor
    • children under 12 years: do not use this adult extra strength product in children under 12 years of age; this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage

  • Other information

    • store at 25ºC (77ºF); excursions permitted between 15°-30°C (59°-86°F)
    • see end flap for expiration date and lot number

  • Inactive ingredients

    caster oil, hypromellose, povidone, sodium starch glycolate*, starch, stearic acid

    *may contain this ingredient


  • PRODUCT PACKAGING

    Pain Reliever/Fever Reducer

    Compare to the Active Ingredient in Tylenol® Extra Strength Caplets†

    Our Family®
    Quality Care Since 1904

    PAIN RELIEVER
    ACETAMINOPHEN
    EXTRA STRENGTH

    24 CAPLETS

    500 mg EACH

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

    †This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Tylenol® Extra Strength Caplets.
     50844       REV0213B17508

    DISTRIBUTED BY
    NASH FINCH COMPANY ©2004, 1996
    NFC BRANDS
    7600 FRANCE AVE S,MPLS, MN 55435
    www.ourfamilyfoods.com           NF18229

    Our Family 44-175

    Our Family 44-175


  • INGREDIENTS AND APPEARANCE
    PAIN RELIEVER 
    acetaminophen tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:70253-175
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg
    Inactive Ingredients
    Ingredient Name Strength
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    POVIDONES (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    Product Characteristics
    Color WHITE Score no score
    Shape CAPSULE (Tablet) Size 18mm
    Flavor Imprint Code 44;175
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:70253-175-08 1 in 1 CARTON
    1 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2 NDC:70253-175-12 1 in 1 CARTON
    2 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3 NDC:70253-175-15 1 in 1 CARTON
    3 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4 NDC:70253-175-14 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part343 04/02/1993 04/02/2018
    Labeler - NASH-FINCH COMPANY (006962294)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867894 MANUFACTURE(70253-175)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 038154464 PACK(70253-175)