warnings
Warnings Do not use laxative products for longer than 1 week unless directed by a doctor
Senokot
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Senokot
- Generic name
- STANDARDIZED SENNA CONCENTRATE
- Manufacturer
- Atlantis Consumer Healthcare, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d5bf67e5-82c6-edbf-e9ec-e027fdd47c84
- SPL ID
- 8319c8b6-8d3f-416d-a864-39cb879df2da
- Version
- 11
- Effective date
- 2025-08-20
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:54:20
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M007 | openfda.application_number | |
| brand name | Senokot | openfda.brand_name | |
| generic name | STANDARDIZED SENNA CONCENTRATE | openfda.generic_name | |
| manufacturer name | Atlantis Consumer Healthcare, Inc. | openfda.manufacturer_name | |
| ndc | package | 67618-120-72 | openfda.package_ndc |
| ndc | package | 67618-120-36 | openfda.package_ndc |
| ndc | package | 67618-120-12 | openfda.package_ndc |
| ndc | package | 67618-120-73 | openfda.package_ndc |
| ndc | package | 67618-120-06 | openfda.package_ndc |
| ndc | product | 67618-120 | openfda.product_ndc |
| ndc11 | package | 67618012073 | derived:openfda.package_ndc |
| ndc11 | package | 67618012036 | derived:openfda.package_ndc |
| ndc11 | package | 67618012072 | derived:openfda.package_ndc |
| ndc11 | package | 67618012012 | derived:openfda.package_ndc |
| ndc11 | package | 67618012006 | derived:openfda.package_ndc |
| rxcui | 1039965 | openfda.rxcui | |
| rxcui | 602802 | openfda.rxcui | |
| spl id | 8319c8b6-8d3f-416d-a864-39cb879df2da | id | |
| spl set id | d5bf67e5-82c6-edbf-e9ec-e027fdd47c84 | set_id | |
| unii | 3FYP5M0IJX | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.