Sennosides 8.6 mg

Sennosides 8.6 mg is an FDA-registered drug product whose active ingredient is SENNOSIDES. It is labelled by Morepen Bio Inc taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 87717-501, application M007, label effective 20260905. It is one of 20 FDA drug label records sharing the active ingredient SENNOSIDES. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing SENNOSIDES are most often described in connection with: usage indications. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Indications and Usage Indications & Usage

Dosage and Administration Dosage & Administration

Warnings Warnings Keep out of Reach of Children Keep out of Reach of Children

FDA lists 20 drug label records with SENNOSIDES as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Sennosides 8.6 mg used for?
Indications and Usage Indications & Usage

Who makes Sennosides 8.6 mg?
Morepen Bio Inc is the labeler of record for Sennosides 8.6 mg. 20 FDA label records share the active ingredient SENNOSIDES, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Sennosides 8.6 mg come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Sennosides 8.6 mg prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing SENNOSIDES?
Yes. 20 FDA drug label records list SENNOSIDES as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Sennosides 8.6 mg been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.