Label: SENNA SYRUP- natural vegetable laxative liquid

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

Drug Label Information

Updated December 16, 2024

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  • Active Ingredients

    Sennosides 8.8 mg

  • Purpose

    Laxative

  • Warning

    Do not use laxative products for longer than 1 week
    unless directed by a doctor.

  • Uses

    • Relieves occasional constipation (irregularity)
    • Generally causes bowel movement in 6 to 12 hours

  • Ask a doctor before use if you

    • have stomach pain, nausea or vomiting
    • notice a change in bowel habits that last over 2 weeks
    • are pregnant or breastfeeding.

  • Stop Use and ask a doctor

    if you have rectal bleeding or failure to have a bowel movement after use.

  • Keep out of Reach of Children

    In case of accidental overdose, get medical help or contact a Poison Control Center immediately.

  • Directions

    Shake well before using. Do not exceed maximum dose. Take at bedtime or as directed by a doctor.

  • OTHER SAFETY INFORMATION

    Store at controlled room temperature 20-25°C(68-77°F). Excursions permitted 15-30° (59-86°F).
    Tamper Evident: Do not use if foil seal over bottle opening is torn, broken or missing.

  • Inactive Ingredients


    Chocolate flavor, methylparaben, propylene glycol, proylparaben, purified water and sucrose

  • Dosage

    AgeUsual DoseMaximum Dose
    Adults and Children 12 years and older2-3 teaspoons once a day3 teaspoons twice a day
    6-12 years1 to 1 1/2 teaspoons once a day1 1/2 teaspoons twice a day
    2-6 years1/2 to 3/4 teaspoon once a day3/4 teaspoons twice a day
    under 2 yearsConsult a doctor

  • HOW SUPPLIED

    Senna Syrup 8.8 mg/5 mL

    • NDC 63629-9268-1: 237 mL in a BOTTLE

    Repackaged/Relabeled by:
    Bryant Ranch Prepack, Inc.
    Burbank, CA 91504

  • PRINCIPAL DISPLAY PANEL

    Senna Syrup 8.8 mg/5 mL

    Label
  • INGREDIENTS AND APPEARANCE
    SENNA SYRUP 
    natural vegetable laxative liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63629-9268(NDC:58657-518)
    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
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SUCROSE (UNII: C151H8M554)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63629-9268-1237 mL in 1 BOTTLE; Type 0: Not a Combination Product04/04/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00709/28/2021
    Labeler - Bryant Ranch Prepack (171714327)
    Registrant - Bryant Ranch Prepack (171714327)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bryant Ranch Prepack171714327REPACK(63629-9268) , RELABEL(63629-9268)
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