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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 250 PACKET in 1 BOX, UNIT-DOSE (47682-810-13) > 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

Complete Medi First Cramp Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredients (in each tablet)

    Acetaminophen 325 mg

    Pamabrom 25 mg


  • Purposes

    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

    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.

    If pregnant or breast-feeding, ask a health professional before use.


  • 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


  • Principal Display Panel - 810R MFP Cramp Tabs

    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

    MFP Cramp Tabs


  • 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

    MF Cramp Tabs


  • Otis Clapp Femcaps

    Otis Clapp

    Quality and Integrity Since 1840

    FEMCAPS â„¢

    Dysmenorrhea Reliever

    New Formula

    See Warnings and Directions on Side Panel

    See new warnings information

    Acetaminophen 325 mg,

    Pamabrom 25 mg

    Tear Out Along Perforation To Dispense

    PROFESSIONAL HEALTHCARE

    300 Tablets (150 PACKETS OF 2)

    Cramp


  • 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
    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
    OTIS CLAPP FEMCAPS 
    acetaminophen, pamabrom tablet, film coated
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-578
    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:47682-578-03 150 in 1 BOX, UNIT-DOSE 12/30/2008 03/10/2015
    1 NDC:47682-578-99 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 03/10/2015
    Labeler - Unifirst First Aid Corporation (832947092)