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SennaStandardized Senna Concentrate 8.6 mg Sennosides Each

Dosage form
TABLET, FILM COATED
Labeler
medsource pharmaceuticals
Label updated
2019-12-30
Retrieved
2026-09-07
Active ingredients
SENNOSIDES
View original label and images on DailyMed ↗
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
Warnings

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
age starting dosage maximum 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
ask a doctor
ask a doctor
Other information
  • Each tablet contains: Calcium 20 mg
  • Store at room temperature
  • Do not use if imprinted seal under cap is broken or missing
Inactive ingredients

Calcium carbonate, croscarmellose sodium, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, propylene glycol, silicon dioxide, sodium sulfate, stearic acid, triacetin.

Questions?

If you have any questions or comments,or to report an adverse event, please contact (800) 795-9775.

Principal Display Panel

[Image in the official label — see DailyMed source]

DailyMed Set ID: 9af0e21e-0667-4c83-e053-2995a90a2f0f · Version 1
NDC: 45865-974