Skip to Content

Humco Senna Leaves

Dosage form: extract
Ingredients: SENNOSIDES A AND B 1000mg in 1g
Labeler: Humco Holding Group, Inc.
NDC Code: 0395-2649

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Humco Senna Leaves

Drug Facts

Active Ingredient

Senna Leaves


Stimulant laxative


For the temporary relief of occasional constipation. Bowel movement is generlly produced in 6 to 12 hours.


Do not use when abdominal pain, nausea, or vomiting are present unless directed by a doctor. Frequent or prolonged use may result in the dependence on laxatives.

Ask a doctor before use

if you have noticed a sudden change in bowel habits that persits over a period of 2 weeks. Laxative product should not be used for a period of longer than 1 week unless directed by a doctor.

When using this product

Discontinie use and consult a doctor if you have rectal bleeding or failure to hav a bowel movement after the use of a laxative. These symptoms 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 accidental overdose, seek professional assistance or contact a Poison Control Center immediately.


Adults and children 12 yrs. of age and older: oral dose is 1 to 3 teaspoonful of tea (prepared as indicated below) once or twice daily or as directed by a doctor.

not recommended for Children under 12 yrs. of age. Consult a doctor before use.

Prepare a tea by steeping 1 ounce of rinsed Senna Leaves in one pint boiling water; let stand 1 hour. Then strain. Press out all the liquid and discard leaves.

Inactive Ingredient


Principal display panel

Label 16 oz

senna leaves extract
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-2649
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:0395-2649-94113 g in 1 BOTTLE, PLASTIC
2NDC:0395-2649-01454 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33403/25/1998
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Humco Holding Group, Inc825672884manufacture(0395-2649), analysis(0395-2649), pack(0395-2649), label(0395-2649)

Revised: 11/2017
Humco Holding Group, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.