Home > Drugs A-Z > Medi First Cramp

Medi First Cramp (Unifirst First Aid Corporation)

Available Formats

Dosage Form Package Information Links
TABLET, FILM COATED 125 PACKET in 1 BOX, UNIT-DOSE (47682-810-48) > 2 TABLET, FILM COATED in 1 PACKET (47682-810-99) Label Information
TABLET, FILM COATED 50 PACKET in 1 BOX, UNIT-DOSE (47682-810-33) > 2 TABLET, FILM COATED in 1 PACKET (47682-810-99) Label Information
TABLET, FILM COATED 250 PACKET in 1 BOX, UNIT-DOSE (47682-810-13) > 2 TABLET, FILM COATED in 1 PACKET (47682-810-99) Label Information

Complete Medi First Cramp Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredients (in each tablet)

    Acetaminophen 325 mg

    Pamabrom 25 mg


  • Purpose

    Pain reliever/fever reducer

    Diuretic


  • Uses

    For the temporary relief of minor aches and pains associated with

    • headache
    • backaches
    • menstrual cramps

    Temporarily relieves water-weight gain, bloating, swelling and full feeling associated with the premenstrual and menstrual periods.


  • Warnings

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

    â–  more than 4,000 mg of acetaminophen in 24 hours

    â–  with other drugs containing acetaminophen

    â–  3 or more alcoholic drinks every day while using this product

    Allergy alert:

    acetaminophen may cause severe skin reactions. Symptoms may include:

    â–  skin reddening

    â–  blisters

    â–  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.
    • for more than 10 days for pain unless directed by a doctor
    • for more than 3 days for fever unless directed by a doctor

    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 using and ask a doctor if
    • symptoms do not improve
    • new symptoms occur
    • pain or fever persists or gets worse
    • 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 accidental overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.


  • Directions

    • do not use more than directed

    Adults and children: (12 years and older)

    Take 2 tablets every 4 to 6 hours as needed. Do not take more than 8 tablets in 24 hours.

    Children under 12 years:

    Do not give to children under 12 years of age.


  • Other information

    • read all product information before using
    • store at room temperature 59º-86ºF (15º-30ºC)
    • avoid excessive heat and humidity
    • tamper-evident sealed packets
    • do not use any opened or torn packets

  • Inactive ingredients

    corn starch, D&C yellow #10, FD&C blue #1, FD&C red #40, microcrystalline cellulose, povidone, stearic acid, sucrose


  • Questions or comments?

    1-800-634-7680


  • Medi-First Plus Cramp Tabs Label

    100 Tablets

    (50 x 2's)

    Medi First® Plus

    Cramp Tabs

    Acetaminophen 325 mg / Pamabrom 25 mg

    Pull to Open

    Menstrual Relief

    Tamper Evident Unit Dose Packets

    Medi-First Plus


  • Principal Display Panel MF Cramp Tabs

    100 Tablets

    (50 x 2)

    Medi-First®

    Cramp Tabs

    Menstrual Pain Relief

    Pull to Open

    Pain Reliever Acetaminophen 325 mg

    Diuretic Pamabrom 25 mg

    Tamper Evident

    Unit Dose Packets

    edi-First Cramp Tabs


  • INGREDIENTS AND APPEARANCE
    MEDI FIRST CRAMP 
    acetaminophen, pamabrom tablet, film coated
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-810
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    PAMABROM (UNII: UA8U0KJM72) (BROMOTHEOPHYLLINE - UNII:FZG87K1MQ6) PAMABROM 25 mg
    Inactive Ingredients
    Ingredient Name Strength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    POVIDONE (UNII: FZ989GH94E)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    Color white (white) Score no score
    Shape ROUND (ROUND) Size 11mm
    Flavor Imprint Code FR;7
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-810-33 50 in 1 BOX, UNIT-DOSE 12/30/2008
    1 2 in 1 PACKET; Type 0: Not a Combination Product
    2 NDC:47682-810-48 125 in 1 BOX, UNIT-DOSE 12/30/2008
    2 2 in 1 PACKET; Type 0: Not a Combination Product
    3 NDC:47682-810-13 250 in 1 BOX, UNIT-DOSE 12/30/2008
    3 NDC:47682-810-99 2 in 1 PACKET; Type 0: Not a Combination Product
    4 NDC:47682-810-99 2 in 1 PACKET; Type 0: Not a Combination Product 12/30/2008
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part343 12/30/2008
    MEDI FIRST PLUS CRAMP 
    acetaminophen, pamabrom tablet, film coated
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-910
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    PAMABROM (UNII: UA8U0KJM72) (BROMOTHEOPHYLLINE - UNII:FZG87K1MQ6) PAMABROM 25 mg
    Inactive Ingredients
    Ingredient Name Strength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    POVIDONE (UNII: FZ989GH94E)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    Color white (white) Score no score
    Shape ROUND (ROUND) Size 11mm
    Flavor Imprint Code FR;7
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-910-33 50 in 1 BOX, UNIT-DOSE 12/30/2008
    1 2 in 1 PACKET; Type 0: Not a Combination Product
    2 NDC:47682-910-48 125 in 1 BOX, UNIT-DOSE 12/30/2008
    2 2 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part343 12/30/2008
    Labeler - Unifirst First Aid Corporation (832947092)