Label: SENNA SYRUP- sennosides liquid

  • NDC Code(s): 54859-808-08
  • Packager: Llorens Pharmaceutical International Division, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 23, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Per teaspoonful-5mL

    Sennosides - 8.8 mg

  • PURPOSE

    Purpose

    Laxative

  • INDICATIONS & USAGE

    Uses

    • relieves occasional constipation (irregularity)
    • generally causes bowel movment in 6 to 12 hours
  • WARNINGS

    Warnings

    Do not use

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

    Ask a doctor or pharmacis before use if you have

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

    Stope use and ask a doctor if

    you have rectal bleeding or failure to have a bowel movemebt after use of laxative. They may indicate a serious condition.

  • PREGNANCY

    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 accidental overdose, get medical help or contact a Poison Control Center immediately

  • DOSAGE & ADMINISTRATION

    • shake well before use
    • Do not exceed recommended dose
     Age Starting Dose Maximum dosage
     Adults and children 12 years and older 2-3 teaspoonfuls once a day preferably at bedtime; increase as needed or as recommended by a doctor3 teaspoons in the morning and 3 teaspoons at bedtime
    Under 12 years of age ask a doctor ask a doctor

  • INACTIVE INGREDIENT

    Inactive ingredients artificial and natural chocolate flavor, methylparaben, propylene glycol, propylparaben, purified water, and sucrose.

  • QUESTIONS

    Questions or comments? 1-866-595-5598

  • PRINCIPAL DISPLAY PANEL

    Senna

  • INGREDIENTS AND APPEARANCE
    SENNA SYRUP 
    sennosides liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54859-808
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.8 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54859-808-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00705/01/2019
    Labeler - Llorens Pharmaceutical International Division, Inc. (037342305)
    Registrant - Llorens Pharmaceutical International Division, Inc. (037342305)