Home > Drugs A-Z > Up and Up anti diarrheal

Up and Up anti diarrheal (Target Corporation)

Available Formats

Dosage Form Package Information Links
TABLET 4 BLISTER PACK in 1 CARTON (11673-224-62) > 6 TABLET in 1 BLISTER PACK Label Information
TABLET 1 BOTTLE in 1 CARTON (11673-224-67) > 48 TABLET in 1 BOTTLE Label Information

Complete Up and Up anti diarrheal Information

  • Active ingredient (in each caplet)

    Loperamide HCl 2 mg


  • Purpose

    Anti-diarrheal


  • Use

    controls 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

    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
    • 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 for 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
    • find right dose on chart. If possible, use weight to dose; otherwise, use age.

    adults and children

    12 years and over

    2 caplets after the first loose stool; 1 caplet after each subsequent loose stool; but no more than 4 caplets in 24 hours

    children 9-11 years

    (60-95 lbs)

    1 caplet after the first loose stool; 1/2 caplet after each subsequent loose stool; but no more than 3 caplets in 24 hours

    children 6-8 years

    (48-59 lbs)

    1 caplet after the first loose stool; 1/2 caplet after each subsequent loose stool; but no more than 2 caplets in 24 hours

    children 2-5 years

    (34 to 47 lbs)

    ask a doctor

    children under 2 years

    (up to 33 lbs)

    do not use


  • Other information

    • store at 20°-25°C (68°-77°F)
    • see end panel for lot number and expiration date

  • Inactive ingredients

    anhydrous lactose, carnauba wax, D&C yellow no. 10 aluminum lake, FD&C blue no. 1 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized starch


  • Questions? Call

    1-888-547-7400


  • Principal Display Panel

    see new warning and directions

    Compare to active ingredient in Imodium® A-D

    loperamide hydrochloride tablets, 2 mg

    anti-diarrheal

    controls the symptoms of diarrhea

    anti-diarrheal

    ACTUAL SIZE

    24 CAPLETS*

    24 CAPLETS*

    (*CAPSULE-SHAPED TABLETS)

    224UW-anti-diarrheal-image1.jpg
    224UW-anti-diarrheal-image2.jpg

  • INGREDIENTS AND APPEARANCE
    UP AND UP ANTI DIARRHEAL 
    loperamide hydrochloride tablet, film coated
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-224
    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)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    Color GREEN Score 2 pieces
    Shape OVAL Size 10mm
    Flavor Imprint Code L2
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-224-62 24 in 1 CARTON 07/20/2009 12/18/2014
    1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2 NDC:11673-224-67 1 in 1 CARTON 07/21/2009
    2 48 in 1 BOTTLE; Type 0: Not a Combination Product
    3 NDC:11673-224-02 1 in 1 CARTON 01/03/2013
    3 24 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA075232 07/20/2009
    Labeler - Target Corporation (006961700)