SUNMARK PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [MCKESSON]

  • Home
  • SUNMARK PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [MCKESSON]

SUNMARK PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [MCKESSON]
PDF | XML
NDC 49348-042-09, 49348-042-10, 49348-042-14, 49348-042-19, 49348-042-42
Set ID 8d2e3941-f3c4-4181-871b-3cf6a6cdd3e0
Category HUMAN OTC DRUG LABEL
Packager Strategic Sourcing Services LLC
Generic Name
Product Class
Product Number
Application Number PART343
View All Sections
  • Active ingredient (in each caplet)

    Acetaminophen 500 mg

  • Purpose

    Pain reliever/fever reducer

  • Uses

    •
    temporarily relieves minor aches and pains due to:
    •
    the common cold
    •
    headache
    •
    backache
    •
    minor pain of 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:

    •
    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 have ever had an allergic reaction to this product or any of its ingredients

    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 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 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 years

    ask a doctor
  • Other information

    •
    store at 20-25ºC (68-77ºF)
  • Inactive ingredients

    carnauba wax, corn starch*, croscarmellose sodium*, hypromellose, polyethylene glycol, povidone, pregelatinized starch, sodium starch glycolate*, stearic acid

    *may contain one or more of these ingredients

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    COMPARE TO EXTRA STRENGTH TYLENOL® ACTIVE INGREDIENT

    pain reliever

    Extra Strength

    Pain reliever/Fever reducer

    Adults

    Acetaminophen

    Actual Size

    50 CAPLETS 500 mg EACH

    GLUTEN FREE

    484-s1-pain-reliever.jpg
  • INGREDIENTS AND APPEARANCE
    SUNMARK PAIN RELIEVER  EXTRA STRENGTH
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-042
    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)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize16mm
    FlavorImprint Code L484
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49348-042-091 in 1 CARTON08/11/2003
    150 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:49348-042-101 in 1 CARTON08/11/2003
    2100 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:49348-042-14500 in 1 BOTTLE; Type 0: Not a Combination Product08/11/2003
    4NDC:49348-042-191 in 1 CARTON08/11/200305/15/2014
    4250 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:49348-042-42550 in 1 BOTTLE; Type 0: Not a Combination Product08/11/200303/15/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34308/11/2003
    Labeler - Strategic Sourcing Services LLC (116956644)
View All Sections

Related Drugs

Search DailyMed Drugs