Label: PREMSYN PMS PREMENSTRUAL PAIN RELIEF- acetaminophen and pamabrom and pyrilamine maleate tablet

  • NDC Code(s): 71687-3102-4
  • Packager: Focus Consumer Healthcare, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 10, 2020

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

  • ACTIVE INGREDIENT

    (in each caplet)

    Acetaminophen 500 mg

    Pamabrom 25 mg

    Pyrilamine maleate 15 mg

  • PURPOSE

    Pain reliever

    Antihistamine

    Diuretic

  • INDICATIONS & USAGE

    For the temporary relief of these symptoms associated with menstrual periods:

    • cramps
    • headache
    • bloating
    • backache
    • water-weight gain
    • muscular aches
    • irritability
  • WARNINGS

    Allergy Warning: 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.

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

    more than 8 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



    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
    • glaucoma
    • a breathing problem such as emphysema or chronic bronchitis
    • difficulty in urination due to enlargment of the prostate gland.

    Ask a doctor or pharmacist before use if you are:

    • taking the blood thinning drug warfarin
    • taking sedatives or tranquilizers
    • When using this product,
    • you may get drowsy, avoid alcoholic beverages
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • use caution when driving or operating machinery
    • excitability may occur, especially in children

    stop use and ask doctor if:

    • Pain gets worse or lasts for more than 10 days
    • fever gets worse or lasts for more than 3 days
    • new symptoms occur
    • redness or swelling is present
    • If pregnant or breastfeeding, ask a health professional before use.

    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
    • glaucoma
    • a breathing problem such as emphysema or chronic bronchitis
    • difficulty in urination due to enlargement of the prostate gland

    Ask a doctor or pharmacist before use

    if you are

    • taking the blood thinning drug warfarin 
    • taking sedatives or tranquilizers

    When using this product

    • you may get drowsy, avoid alcoholic beverages
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • use caution when driving or operating machinery
    • excitability may occur, especially in children

    Stop use and ask a doctor if

    • pain gets worse or lasts for more than 10 days
    • fever gets worse or lasts for more than 3 days
    • new symptoms occur
    • redness or swelling is present

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get medical help or contact a poison control center right away.

    Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • DOSAGE & ADMINISTRATION

    adults and children 12 years and over:

    • take 2 caplets with water every 6 hours as needed
    • do not exceed 8 caplets in a 24 hour period or as directed by a doctor
    • do not use more than directed (see warnings)

    children under 12 years: ask a doctor

  • INACTIVE INGREDIENT

    blue 2, candelilla wax, corn starch, ethylparaben, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, pregalatinized starch, propylaparaben, red 40, sodium starch glycolate, stearic acid, talc, titanium dioxide

  • PRINCIPAL DISPLAY PANEL

    label1

  • INGREDIENTS AND APPEARANCE
    PREMSYN PMS PREMENSTRUAL PAIN RELIEF 
    acetaminophen and pamabrom and pyrilamine maleate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71687-3102
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    PAMABROM (UNII: UA8U0KJM72) (BROMOTHEOPHYLLINE - UNII:FZG87K1MQ6) PAMABROM25 mg
    PYRILAMINE MALEATE (UNII: R35D29L3ZA) (PYRILAMINE - UNII:HPE317O9TL) PYRILAMINE MALEATE15 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSPOVIDONE (UNII: 68401960MK)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POVIDONE (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    Colorpurple (FD & C Red No. 40) Scoreno score
    ShapeOVALSize18mm
    FlavorImprint Code P
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71687-3102-41 in 1 CARTON10/13/2017
    140 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34310/13/2017
    Labeler - Focus Consumer Healthcare, LLC (080743737)