Label: DG HEALTH PAIN RELIEF- acetaminophen tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 2, 2024

If you are a consumer or patient please visit this version.

  • Active ingredient (in each tablet)

    Acetaminophen 325 mg

  • Purpose

    Pain reliever/fever reducer

  • Uses

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

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if

    adult takes more than 4,000 mg of acetaminophen in 24 hours
    child takes more than 5 doses in 24 hours
    taken with other drugs containing acetaminophen
    adult has 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 the user has ever had an allergic reaction to this product or any of its ingredients

    Ask a doctor before use if the user

    has liver disease
    is a child with pain of arthritis

    Ask a doctor or pharmacist before use if the user is

    taking the blood thinning drug warfarin

    Stop use and ask a doctor if

    pain gets worse or lasts more than 10 days (for adults) or 5 days (for children)
    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

    do not take more than directed (see overdose warning)

    adults and children 12 years and over

    take 2 tablets every 4 to 6 hours while symptoms last
    do not take more than 10 tablets in 24 hours
    do not use for more than 10 days unless directed by a doctor

    children

    6-11 years

    take 1 tablet every 4 to 6 hours while symptoms last
    do not take more than 5 tablets in 24 hours
    do not use for more than 5 days unless directed by a
     
    doctor

    children under

    6 years

    ask a doctor

  • Inactive ingredients

    croscarmellose sodium*, povidone, pregelatinized starch, stearic acid

    *may contain this ingredient

  • Questions or comments?

    1-888-309-9030

  • Principal Display Panel

    Compare to the active ingredient of Regular Strength Tylenol® Tablets

    Regular Strength

    Pain Relief

    Acetaminophen, 325 mg

    Pain Reliever/Fever Reducer

    100 Tablets

    325 mg

    For ages 6 years and over

    Actual Tablet Size

    Regular Strength Pain Relief Carton Image 1
    Regular Strength Pain Relief Carton Image 2
  • INGREDIENTS AND APPEARANCE
    DG HEALTH PAIN RELIEF 
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-697
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeROUND (beveled edge) Size10mm
    FlavorImprint Code 325MG;L403
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55910-697-781 in 1 CARTON07/01/2019
    1100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01307/01/2019
    Labeler - Dolgencorp, LLC (068331990)