Bisacodyl is an over-the-counter medicine (Stimulant Laxative). The sections below reproduce one FDA label for it, named under "Label". Products in other forms, strengths or from other makers have their own labels, which can differ.
- Type
- Over the counter (OTC)
- Brand names
- Gentle Laxative, Womens Gentle Laxative, stimulant laxative enteric coated, Laxative Enteric Coated, Laxative Gentle, Dulcolax Laxative, Fleet
- Drug class
- Stimulant Laxative
- Taken
- Oral
- Label
- KROGER COMPANY, revised September 9, 2026 · full label on DailyMed
Purpose
Stimulant laxative
What it is used for
relieves occasional constipation and irregularity this product generally produces a bowel movement in 6 to 12 hours
Active ingredient
Active ingredeint (in each tablet) Bisacodyl 5 mg
Do not use
if you cannot swallow without chewing
Ask a doctor before use if you have
stomach pain, nausea or vomiting noticed a sudden change in bowel habits that lasts more than 2 weeks
When using this product
it may cause stomach discomfort, faintness and cramps do not chew or crush tablet(s) do not use within 1 hour after taking an antacid or milk
Stop use and ask a doctor if
you have rectal bleeding or fail to have a bowel movement after using this product. These could be signs of a serious condition. you need to use a laxative for more than 1 week
Pregnancy or breastfeeding
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 (1-800-222-1222).
Dosage:
we do not reproduce dosing instructions. The right dose depends on the person and the condition and is set by the prescriber or pharmacist. Dosage section of the full label.
Bisacodyl in the news
We have not covered this medicine yet. Latest news
Recalls
No recalls matched to this medicine in FDA enforcement reports from the last 3 years (or older ones still open). Search all recalls
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Source: FDA structured product labeling, retrieved through openFDA. Label text is shown as published by the FDA, without editing; long sections are shortened, marked […]. openFDA data are not validated for clinical use — always check the current label and ask a doctor or pharmacist about your own treatment. Set ID a13a8eec-3652-8c57-e053-2995a90aaebf.