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Regular Strength QPAP (Bryant Ranch Prepack)

Available Formats

Dosage Form Package Information Links
TABLET 60 TABLET in 1 BOTTLE (63629-1518-7) Label Information
TABLET 100 TABLET in 1 BOTTLE (63629-1518-2) Label Information
TABLET 6 TABLET in 1 BOTTLE (63629-1518-5) Label Information
TABLET 10 TABLET in 1 BOTTLE (63629-1518-6) Label Information
TABLET 20 TABLET in 1 BOTTLE (63629-1518-1) Label Information
TABLET 30 TABLET in 1 BOTTLE (63629-1518-3) Label Information
TABLET 2 TABLET in 1 BOTTLE (63629-1518-4) Label Information

Complete Regular Strength QPAP Information

  • Active ingredient (in each tablet)

    Acetaminophen 325 mg


  • Purpose

    Pain reliever/ fever reducer


  • Uses

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

  • Warnings

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

    • adult takes more than 12 tablets in 24 hours, which is the maximum daily amount
    • 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

  • 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 DOCTOR

    Ask a doctor before use if the user has liver disease


  • ASK DOCTOR/PHARMACIST

    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 in adults and children
    • pain gets worse or lasts more than 5 days in children under 12 years
    • 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.


  • PREGNANCY OR BREAST FEEDING

    If pregnant or 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 damage. 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 12 tablets in 24 hours

    children 6 years to 11 years

    • take 1 tablet every 4 to 6 hours while symptoms last
    • do not take more than 5 tablets in 24 hours
    children under 6 years do not use adult Regular Strength product in children under 6 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage

  • Inactive ingredients

    povidone, pregelatinized starch, stearic acid


  • Acetaminophen 325 mg. Tablet

    Image File

  • INGREDIENTS AND APPEARANCE
    REGULAR STRENGTH QPAP 
    acetaminophen tablet
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63629-1518(NDC:0603-0263)
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    Inactive Ingredients
    Ingredient Name Strength
    POVIDONES (UNII: FZ989GH94E)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    Color WHITE Score 2 pieces
    Shape ROUND Size 10mm
    Flavor Imprint Code 0027;V
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63629-1518-1 20 in 1 BOTTLE
    2 NDC:63629-1518-2 100 in 1 BOTTLE
    3 NDC:63629-1518-3 30 in 1 BOTTLE
    4 NDC:63629-1518-4 2 in 1 BOTTLE
    5 NDC:63629-1518-5 6 in 1 BOTTLE
    6 NDC:63629-1518-6 10 in 1 BOTTLE
    7 NDC:63629-1518-7 60 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part343 02/01/1996
    Labeler - Bryant Ranch Prepack (171714327)
    Registrant - Bryant Ranch Prepack (171714327)
    Establishment
    Name Address ID/FEI Business Operations
    Bryant Ranch Prepack 171714327 REPACK(63629-1518) , RELABEL(63629-1518)