Senokot-S
Senokot-S is an FDA drug label for the active ingredient STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM manufactured by Atlantis Consumer Healthcare, Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260821.
- Generic name
- STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM
- Manufacturer
- Atlantis Consumer Healthcare, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 67618-310
- Application
- M007
- Label effective
- 20260821
About this product
Senokot-S is an FDA-registered drug product whose active ingredient is STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM. It is labelled by Atlantis Consumer Healthcare, Inc. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 67618-310, application M007, label effective 20260821. 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.
What it is used for
Across FDA labelling, products containing STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM are most often described in connection with: drug facts. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Drug Facts
Dosage & Administration
Directions take preferably at bedtime or as directed by a doctor age startingdosage maximumdosage adults and children 12 years of age and over 2 tablets oncea day 4 tablets twicea day children 6 to under 12 years 1 tablet once a day 2 tablets twice a day children 2 to under 6 years 1/2 tablet once a day 1 tablet twice a day children under 2 years ask a doctor ask a doctor
Warnings
Warnings
Frequently asked questions
What is Senokot-S used for?
Drug Facts
Who makes Senokot-S?
Atlantis Consumer Healthcare, Inc. is the labeler of record for Senokot-S.
What form does Senokot-S 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 Senokot-S 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.
Has Senokot-S 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.