FDA Label for Senna-lax

View Indications, Usage & Precautions

Senna-lax Product Label

The following document was submitted to the FDA by the labeler of this product Bryant Ranch Prepack. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Active Ingredient (In Each Tablet)



Sennosides 8.6 mg


Purpose



Laxative


Uses



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

Do Not Use



  • 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 continues over a period of 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
  • agestarting dosagemaximum dosage
    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 of age
    1 tablet once a day
    2 tablets twice a day
    children 2 to under 6 years of age
    1/2 tablet once a day
    1 tablet twice a day
    children under 2 years of age
    ask a doctor
    ask a doctor

Inactive Ingredients



Acacia Gum, Calcium Carbonate, Croscarmellose Sodium, Dextrose, Hypromellose, Magnesium Stearate, Maltodextrin, Microcrystalline Cellulose, Propylene Glycol, Silicon Dioxide, Stearic Acid, Triacetin.


Questions?



Adverse Drug Event call (800) 616-2471


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