Label: SENNOSIDES tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 12, 2024

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Sennosides

  • Purpose

    Laxative

  • Keep out of Reach of Children

    In case of accidental overdose, contact a doctor or Poison Control Center immediately.

  • Uses

    For relief of occasional constipation and irregularity.

    This product produces a bowel movement in 6 to 12 hours.

  • Warnings

    Do not use laxative products for more than one week unless directed by a doctor

    Ask a doctor before use if you have stomach pains, nausea, vomiting, notice a sudden change in bowel habits that continues over a period of 2 weeks.

    Stop use and ask a doctor ifrectal bleeding or failure to have a bowel movement occur after use of a laxative.  These could be signs of a serious condition.

    If Pregnant or breast-feedingask a health professional before use.

  • Directions

    Take preferably at bedtime or as directed by a doctor.  

    Adults and children over 12 years: 2 tablets once a day.  Maximum of 4 tablets twice a day.

    Children 6 to under 12 years: 1 tablet once a day.  Maximum of 2 tablets twice a day.

    Children 2 to under 6 years: 1/2 tablet once a day.  Maximum of 1 tablet twice a day.

    Children under 2: consult a doctor

  • Inactive Ingredients

    croscarmellose sodium, dibasic dicalcium phosphate, magnesium stearate, microcrystalline cellulose, and silicon dioxide.

  • PRINCIPAL DISPLAY PANEL

    SEN100 Label

  • INGREDIENTS AND APPEARANCE
    SENNOSIDES 
    sennosides tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83813-004
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SENNOSIDES A AND B (UNII: 1B5FPI42EN) (SENNOSIDES A AND B - UNII:1B5FPI42EN) SENNOSIDES A AND B8.6 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    Product Characteristics
    Colorbrown (Speckled various shades of brown) Scoreno score
    ShapeROUND (Round) Size8mm
    FlavorImprint Code CS
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83813-004-06600 in 1 BOTTLE; Type 0: Not a Combination Product04/18/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00704/18/2016
    Labeler - NewVue LLC (119120572)