Psyllium Husk is an over-the-counter medicine. 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
- Metamucil Therapy for regularity
- Taken
- Oral
- Label
- Raritan Pharmaceuticals Inc, revised September 8, 2026 · full label on DailyMed
Purpose
Fiber laxative
What it is used for
- effective in treating occasional constipation and restoring regularity
Active ingredient
Psyllium husk approximately 0.52 g
Warnings
Choking Taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking. Do not take this product if you have difficulty in swallowing. If you experience chest pain, vomiting, or difficulty in swallowing or breathing after taking this product, seek immediate medical attention. Allergy alert This product may cause allergic reaction in people sensitive to inhaled or ingested psyllium. Ask a doctor before use if you have
- a sudden change in bowel habits persisting for 2 weeks
- abdominal pain, nausea or vomiting Stop use and ask a doctor if
- constipation lasts more than 7 days
- rectal bleeding occurs These may be signs of a serious condition. Keep out of reach of children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.
Keep out of reach of children
In case of overdose, get medical help or contact a Poison Control Center right away at 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.
Psyllium husk in the news
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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 22e927bd-5734-424e-8870-1aaa18f1265e.