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Sennosides and Docusate Sodium (McKesson Packaging Services a business unit of McKesson Corporation)

Available Formats

Dosage Form Package Information Links
TABLET 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-432-01) > 30 TABLET in 1 BLISTER PACK Label Information
TABLET 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-432-10) > 10 TABLET in 1 BLISTER PACK Label Information
TABLET 25 BLISTER PACK in 1 BOX (63739-432-04) > 30 TABLET in 1 BLISTER PACK Label Information

Complete Sennosides and Docusate Sodium Information

  • Active ingredient

    Docusate Sodium 50mg

    Sennosides 8.6 mg


  • Purpose

    Docusate Sodium...............Stool Softener

    Sennosides.........................Stimulant Laxative


  • Keep Out of Reach of Children


  • Uses

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

  • Warnings

    Do Not Use
    • this product if you are presently taking mineral oil, unless directed by a doctor
    • laxative products for longer than 1 week unless directed by a doctor

    Ask a doctor before use if you have
    • stomach pain
    • nausea
    • vomiting
    • a sudden change in bowel movements that persists over 2 weeks

    Stop use and ask a doctor if
    • You have rectal bleeding or fail to have a bowel movement after use of a laxative. These could 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

  • Directions

    • Take preferably at bedtime or as directed by a doctor
    • If you do not have a comfortable bowel movement by the second day, increase dose by one tablet (do not exceed the maximum dosage) or decrease dose until you are comfortable.
    Age Starting Dose Maximum Dose
    Adults and children 12 years of age and older 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 tablets twice a day
    Children under 2 years ask a doctor ask a doctor

    Other Information
    • each tablet contains calcium 20mg, sodium 6mg (LOW SODIUM)
    • store at 25°C (77°F)

  • Inactive ingredients

    carnauba wax, colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, D&C yellow #10 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium benzoate, stearic acid, titanium dioxide, **tapioca starch, **tartaric acid

    ** may contain one or more of these ingredients


  • Package/Label Principal Display Panel

    Senna and Docusate label

  • INGREDIENTS AND APPEARANCE
    SENNOSIDES AND DOCUSATE SODIUM 
    sennosides and docusate sodium tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63739-432
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg
    DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 50 mg
    Inactive Ingredients
    Ingredient Name Strength
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    Product Characteristics
    Color ORANGE Score no score
    Shape ROUND Size 5mm
    Flavor Imprint Code TCL;081
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63739-432-10 10 in 1 BOX, UNIT-DOSE
    1 10 in 1 BLISTER PACK
    2 NDC:63739-432-01 25 in 1 BOX, UNIT-DOSE
    2 30 in 1 BLISTER PACK
    3 NDC:63739-432-04 25 in 1 BOX
    3 30 in 1 BLISTER PACK
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved drug other 10/11/2007
    Labeler - McKesson Packaging Services a business unit of McKesson Corporation (140529962)
    Establishment
    Name Address ID/FEI Business Operations
    Time-Cap Labs., Inc. 037052099 MANUFACTURE(63739-432)
    Establishment
    Name Address ID/FEI Business Operations
    McKesson Packaging Services a business unit of McKesson Corporation 140529962 REPACK(63739-432)