Label: SENNA-S- senna and docusate sodium tablets, 8.6 mg and 50 mg tablet, coated

  • NDC Code(s): 69517-131-02, 69517-131-05, 69517-131-10, 69517-131-24, view more
    69517-131-25, 69517-131-50
  • Packager: HealthLife of USA LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 21, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredients Purpose (in each tablet)          Purpose

    Docusate sodium 50 mg.......................................Stool softner

    Sennosides 8.6 mg................................................Laxative

  • Uses

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

    Do not use

    • if you are now 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
    • noticed a sudden change in bowel habits that lasts 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 may indicate 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

    • adults and children 12 years of age or older- starting dosage:2 tablets once a day, maximum dosage:4 tablets twice a day
    • children 6 to under 12 years- starting dosage:1 tablet once a day, maximum dosage:2 tablets twice a day
    • children 2 to under 6 years- starting dosage:1/2 tablet once a day, maximum dosage:1 tablet twice a day
    • children under 2 years- starting dosage:ask a doctor, maximum dosage:ask a doctor
  • Other information

    • each tablet contains: calcium 21 mg
    • each tablet contains: sodium 3 mg VERY LOW SODIUM
    • store at 25ºC (77ºF); excursions permitted between 15°-30°C (59°-86°F)
    • read all product information before using
    • TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
  • Inactive ingredients

    croscarmellose sodium, colloidal silicon dioxide, dicalcium phosphate, D&C Yellow # 10, FD&C Yellow # 6, hypromellose, microcrystalline cellulose, magnesium stearate, maltodextrin, polyethylene glycol, stearic acid, titanium dioxide

  • Questions or comments?

    Call toll free 1-844-832-1138 Monday through Friday 9AM – 5PM EST or www.healthlifeofusa.com

  • PRINCIPAL DISPLAY PANEL

    Compare to the Active Ingredients inSenokot-S®

    *This product is not manufactured or distributed by Purdue Products L.P., owner of the registered trademark Senokot-S®.

    Senna and Docusate Sodium Tablets, 8.6 mg and 50 mg

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    SENNA-S 
    senna and docusate sodium tablets, 8.6 mg and 50 mg tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69517-131
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.6 mg
    DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM50 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColororangeScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code S35
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69517-131-2525 in 1 BOX04/08/2016
    12 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:69517-131-5050 in 1 BOX04/08/2016
    22 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:69517-131-022 in 1 POUCH04/08/2016
    32 in 1 POUCH; Type 0: Not a Combination Product
    4NDC:69517-131-101000 in 1 BOTTLE04/08/2016
    4NDC:69517-131-05500 in 1 BOTTLE
    4NDC:69517-131-2424 in 1 BOTTLE
    41 in 1 CARTON; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/07/2016
    Labeler - HealthLife of USA LLC (079656178)
    Establishment
    NameAddressID/FEIBusiness Operations
    Elysium Pharmaceutical Ltd.915664486manufacture(69517-131)
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