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MEDIQUE Diamode (Unifirst First Aid Corporation)

Available Formats

Dosage Form Package Information Links
TABLET, FILM COATED 6 PACKET in 1 BOX, UNIT-DOSE (47682-200-69) > 1 TABLET, FILM COATED in 1 PACKET (47682-200-46) Label Information
TABLET, FILM COATED 100 PACKET in 1 BOX, UNIT-DOSE (47682-200-33) > 1 TABLET, FILM COATED in 1 PACKET (47682-200-46) Label Information
TABLET, FILM COATED 50 PACKET in 1 BOX, UNIT-DOSE (47682-200-50) > 1 TABLET, FILM COATED in 1 PACKET (47682-200-46) Label Information

Complete MEDIQUE Diamode Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredient (in each caplet)

    Loperamide HCl USP, 2mg


  • Purpose

    Anti-diarrheal


  • Uses

    Controls symptoms of diarrhea, including Travelers' Diarrhea.


  • Warnings

    Allery alert:

    Do not use if you have ever had a rash or other allergic reaction to loperamide HCl.

    Heart alert:

    Taking more than directed can cause serious heart problems or death.

    Do not use
    • if you have bloody or black stool

    Ask a doctor before use if you have
    • a fever
    • mucus in the stool
    • a history of liver disease

    Ask a doctor or pharmacist before use if you are
    • taking antibiotics

    When using this product
    • tiredness, drowsiness or dizziness may occur. Be careful when driving or operating machinery.

    Stop use and ask a doctor if
    • symptoms get worse
    • diarrhea lasts more than 2 days
    • you get abdominal swelling or bulging. These may be signs of a serious condition.

    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 (1-800-222-1222).


  • Directions

    • drink plenty of clear fluids to help prevent dehydration caused by diarrhea

    Adults and children (12 years and over): Take 2 caplets after the first loose stool; 1 caplet after each subsequent loose stool; but no more than 4 caplets in 24 hours.

    Children under 12 years: Do not give to children under 12 years of age.


  • Other information

    • store between 68º - 77ºF (20º - 25ºC)
    • tamper-evident sealed packets
    • do not use any opened or torn packet
    • see back of packet for lot number and expiration date

  • Inactive ingredients

    anhydrous lactose, croscarmellose sodium, crospovidone, D&C Yellow # 10, FD&C Blue # 1, hydrogenated vegetable oil, magnesium stearate, powdered cellulose, pregelatinized starch


  • Questions or comments?

    1-800-634-7680


  • Medique Diamode Label

    Medique ®

    Diamode

    Controls the Symptoms of Diarrhea

    Pull to Open

    See New Warnings Information

    Antidiarrheal Loperamide HCl 2 mg

    50 Caplets

    (50 x 1)

    Tamper Evident Unit Dose Packets

    Medique Diamode Label


  • INGREDIENTS AND APPEARANCE
    MEDIQUE DIAMODE 
    loperamide hydrochloride tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-200
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C) (LOPERAMIDE - UNII:6X9OC3H4II) LOPERAMIDE HYDROCHLORIDE 2 mg
    Inactive Ingredients
    Ingredient Name Strength
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    CROSPOVIDONE (UNII: 68401960MK)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    Color green (Green) Score 2 pieces
    Shape OVAL (Caplet) Size 10mm
    Flavor Imprint Code 123
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-200-69 6 in 1 BOX, UNIT-DOSE 12/30/2008
    1 1 in 1 PACKET; Type 0: Not a Combination Product
    2 NDC:47682-200-50 50 in 1 BOX, UNIT-DOSE 12/30/2008
    2 1 in 1 PACKET; Type 0: Not a Combination Product
    3 NDC:47682-200-33 100 in 1 BOX, UNIT-DOSE 12/30/2008
    3 1 in 1 PACKET; Type 0: Not a Combination Product
    4 NDC:47682-200-46 1 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
    ANDA ANDA074091 12/30/2008
    Labeler - Unifirst First Aid Corporation (832947092)