Label: MEDIQUE DIAMODE- loperamide hydrochloride tablet
PRIVATE LABEL DISTRIBUTOR- loperamide hcl 2 mg tablet

  • NDC Code(s): 47682-021-25, 47682-021-30, 47682-021-50, 47682-021-75, view more
    47682-200-33, 47682-200-46, 47682-200-50, 47682-200-69
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated February 7, 2025

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each caplet)

    Loperamide Hydrochloride 2mg

  • Purpose

    Antidiarrheal

  • Uses

    Controls the symptoms of diarrhea, including Travelers diarrhea.

  • Warnings

    Allergy alert: Do not use if you have ever had a rash or other allergic reaction to Loperamide HCl

    Do not use

    • if you have bloody or black stool

    Ask a doctor before use if you have

    • a fever
    • mucus in 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 you are pregnant or breast feeding, ask a health professional before use.

    Keep this and all drugs out of the reach of children. In case of accidental overdose, contact a physician or Poison Control Center right away.

  • Directions

    • do not use more than directed
    • drink plenty of clear fluids to help prevent dehydration caused by diarrhea

    Adults and children (12 years and older): Take 2 caplets after the first loose stool followed by 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
  • 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

  • Principal Display Panel - 200R Medique Diamode Label

    Medique ®

    Diamode

    Controls the Symptoms of Diarrhea

    Pull to Open

    Antidiarrheal • Loperamide HCl 2 mg

    50 Caplets

    (50 x 1)

    Tamper Evident Unit Dose Packets

    200R Diamode Label

  • Private Label Distributor Physicians Care Anti-Diarrheal

    Physicians Care®

    Anti-Diarrheal

    Controls Symptoms of Diarrhea

    Loperamide Hydrochloride 2 mg

    Pull To Open

    Easy to Swallow

    COATED CAPLETS

    Compare Active ingredient to:

    Imodium AD

    Registered Trademark of McNeil Consumer & Specialty Pharmaceuticals

    Tamper-Evident Unit Dose Packets

    Physicians Care®

    Registered Trademark of ACME UNITED Corporation

    50 PACKETS (1 Caplet 2 Mg Each)

    PC Anti-Diarrheal

  • Private Label Distributor Medex Anti-Diarrheal Relief Principal Display Panel

    Compare to the Active Ingredients in

    Imodium® A-D

    This box contains a generic product called Diamode

    Anti-Diarrheal Relief

    20 Packets of 2 Tablets

    Remove This Panel

    Read Drug Facts and Instructions on Packet

    Anti-Diarrheal Relief

  • INGREDIENTS AND APPEARANCE
    MEDIQUE DIAMODE 
    loperamide hydrochloride tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-200
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C) (LOPERAMIDE - UNII:6X9OC3H4II) LOPERAMIDE HYDROCHLORIDE2 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    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
    Colorgreen (green) Score2 pieces
    ShapeOVAL (Caplet) Size10mm
    FlavorImprint Code 123
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-200-696 in 1 BOX, UNIT-DOSE12/30/2008
    11 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-200-5050 in 1 BOX, UNIT-DOSE12/30/2008
    21 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:47682-200-33100 in 1 BOX, UNIT-DOSE12/30/2008
    3NDC:47682-200-461 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:47682-200-461 in 1 PACKET; Type 0: Not a Combination Product12/30/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07409112/30/2008
    PRIVATE LABEL DISTRIBUTOR 
    loperamide hcl 2 mg tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-021
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C) (LOPERAMIDE - UNII:6X9OC3H4II) LOPERAMIDE HYDROCHLORIDE2 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSPOVIDONE (UNII: 2S7830E561)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorgreenScore2 pieces
    ShapeOVAL (Caplet) Size10mm
    FlavorImprint Code 123
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-021-5050 in 1 BOX, UNIT-DOSE12/30/200812/31/2024
    11 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-021-2525 in 1 BOX, UNIT-DOSE10/01/201512/31/2024
    21 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:47682-021-3030 in 1 BOX, UNIT-DOSE10/01/201512/31/2024
    31 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:47682-021-7575 in 1 BOX, UNIT-DOSE10/01/201512/31/2024
    41 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07409112/30/2008
    Labeler - Unifirst First Aid Corporation (832947092)
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