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Senokot (Purdue Products LP)

Available Formats

Dosage Form Package Information Links
TABLET 2 BLISTER PACK in 1 CARTON (67618-300-20) > 10 TABLET in 1 BLISTER PACK Label Information
TABLET 1 BOTTLE, PLASTIC in 1 CARTON (67618-300-10) > 100 TABLET in 1 BOTTLE, PLASTIC Label Information
TABLET 1 BOTTLE, PLASTIC in 1 CARTON (67618-300-50) > 50 TABLET in 1 BOTTLE, PLASTIC Label Information
TABLET 3 BLISTER PACK in 1 CARTON (67618-300-24) > 24 TABLET in 1 BLISTER PACK Label Information
TABLET 1 BLISTER PACK in 1 CARTON (67618-300-40) > 4 TABLET in 1 BLISTER PACK Label Information
TABLET 4 TABLET in 1 BLISTER PACK (67618-300-04) Label Information

Complete Senokot Information

  • ACTIVE INGREDIENT

    Drug Facts
    Active ingredient (in each tablet)

    Sennosides 8.6 mg


  • PURPOSE

    Laxative


  • INDICATIONS & USAGE

    Uses

    • relieves occasional constipation (irregularity)
    • generally produces a bowel movement in 6-12 hours

  • WARNINGS

    Warnings


  • DO NOT USE

    Do not use

    • laxative products for longer than 1 week unless directed by a doctor

  • ASK DOCTOR/PHARMACIST

    Ask a doctor before use if you have

    • stomach pain
    • nausea
    • vomiting
    • noticed a sudden change in bowel habits that continues over a period of 2 weeks

  • STOP USE

    Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after use of a laxative. These may indicate a serious condition.


  • PREGNANCY OR BREAST FEEDING

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


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.


  • DOSAGE & ADMINISTRATION

    Directions

    • take preferably at bedtime or as directed by a doctor
    age starting dosage maximum dosage
    adults and children
    12 years of age and over
    2 tablets once a day 4 tablets twice a day
    children 6 to under 12 years 1 tablet once a day 2 tablets twice a day
    children 2 to under 6 years 1/2 tablet once a day 1 tablet twice a day
    children under 2 years ask a doctor ask a doctor

  • SPL UNCLASSIFIED SECTION

    Other Information

    • each tablet contains: calcium 10 mg
    • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)

  • INACTIVE INGREDIENT

    Inactive ingredients

    dicalcium phosphate, magnesium stearate, microcrystalline cellulose, pregelatinized starch


  • SPL UNCLASSIFIED SECTION

    ©2016, Purdue Products L.P.



    Mfd. for: Purdue Products L.P., Stamford, CT 06901-3431
    By: Purdue Pharma, 575 Granite Court
    Pickering, ON L1W 3W8, Canada



    304218-0A


  • PRINCIPAL DISPLAY PANEL

    20 Tablets

    304218-0A

  • INGREDIENTS AND APPEARANCE
    SENOKOT 
    standardized senna concentrate tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:67618-300
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg
    Inactive Ingredients
    Ingredient Name Strength
    CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    Color BROWN Score no score
    Shape ROUND Size 9mm
    Flavor Imprint Code S
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:67618-300-40 1 in 1 CARTON 06/01/1956 12/31/2016
    1 4 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2 NDC:67618-300-24 3 in 1 CARTON 06/01/1956 12/31/2016
    2 24 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3 NDC:67618-300-20 2 in 1 CARTON 06/01/1956
    3 10 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4 NDC:67618-300-50 1 in 1 CARTON 06/01/1956
    4 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    5 NDC:67618-300-10 1 in 1 CARTON 06/01/1956
    5 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    6 NDC:67618-300-04 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 06/01/1956 12/31/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part334 06/01/1956
    Labeler - Purdue Products LP (141916531)
    Registrant - Purdue Pharma LP (932323652)
    Establishment
    Name Address ID/FEI Business Operations
    Purdue Pharma 250955291 MANUFACTURE(67618-300)