SUNMARK PAIN RELIEVER (ACETAMINOPHEN) TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]

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  • SUNMARK PAIN RELIEVER (ACETAMINOPHEN) TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]

SUNMARK PAIN RELIEVER (ACETAMINOPHEN) TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]
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NDC 71335-0625-1, 71335-0625-2, 71335-0625-3
Set ID 3026812a-24f7-4051-8111-4fea18f26ff1
Category HUMAN OTC DRUG LABEL
Packager Bryant Ranch Prepack
Generic Name
Product Class
Product Number
Application Number ANDA075077
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  • Active ingredient (in each caplet)

    Acetaminophen 650 mg

  • Purpose

    Pain reliever/fever reducer

  • Uses

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

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

    •
    more than 6 caplets in 24 hours, which is the maximum daily amount
    •
    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 are allergic to acetaminophen or any of the inactive ingredients in this product
  • 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 8 hours with water
    •
    swallow whole; do not crush, chew, split or dissolve
    •
    do not take more than 6 caplets in 24 hours
    •
    do not use for more than 10 days unless directed by a doctor

    children under 12 years
    •
    do not use
  • Other information

    •
    store at 20-25°C (68-77°F)
    •
    do not use if printed foil under cap is broken or missing
    •
    meets the requirements of USP Dissolution Test 2
  • Inactive ingredients

    carnauba wax, colloidal silicon dioxide, croscarmellose sodium, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, polysorbate 80, povidone, pregelatinized starch, stearic acid, titanium dioxide

  • Questions or comments?

    1-800-719-9260

  • HOW SUPPLIED

    Product: 71335-0625

    NDC: 71335-0625-1 30 TABLET, FILM COATED, EXTENDED RELEASE in a BOTTLE

    NDC: 71335-0625-2 100 TABLET, FILM COATED, EXTENDED RELEASE in a BOTTLE

    NDC: 71335-0625-3 50 TABLET, FILM COATED, EXTENDED RELEASE in a BOTTLE

    NDC: 71335-0625-4 60 TABLET, FILM COATED, EXTENDED RELEASE in a BOTTLE

    NDC: 71335-0625-5 120 TABLET, FILM COATED, EXTENDED RELEASE in a BOTTLE

  • Acetaminophen ER 650mg Tablet

    Label Image
  • INGREDIENTS AND APPEARANCE
    SUNMARK PAIN RELIEVER 
    acetaminophen tablet, film coated, extended release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-0625(NDC:70677-0017)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg
    Inactive Ingredients
    Ingredient NameStrength
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize19mm
    FlavorImprint Code L544
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71335-0625-130 in 1 BOTTLE; Type 0: Not a Combination Product05/30/2017
    2NDC:71335-0625-2100 in 1 BOTTLE; Type 0: Not a Combination Product05/30/2017
    3NDC:71335-0625-350 in 1 BOTTLE; Type 0: Not a Combination Product05/30/2017
    4NDC:71335-0625-460 in 1 BOTTLE; Type 0: Not a Combination Product01/19/2018
    5NDC:71335-0625-5120 in 1 BOTTLE; Type 0: Not a Combination Product01/19/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07507705/30/2017
    Labeler - Bryant Ranch Prepack (171714327)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bryant Ranch Prepack171714327REPACK(71335-0625) , RELABEL(71335-0625)
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