warnings
Warnings: Do not use laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor
Maximum Strength Senna Laxative
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
- Maximum Strength Senna Laxative
- Generic name
- SENNOSIDE 25 MG
- Manufacturer
- NUVICARE LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a2a3b83f-2d49-4bc4-90d7-1f2a7f4ea45f
- SPL ID
- caaad95a-c75a-4269-9d46-55a55d9353e6
- Version
- 1
- Effective date
- 2026-01-22
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:47:20
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | Maximum Strength Senna Laxative | openfda.brand_name | |
| generic name | SENNOSIDE 25 MG | openfda.generic_name | |
| manufacturer name | NUVICARE LLC | openfda.manufacturer_name | |
| ndc | package | 84324-033-01 | openfda.package_ndc |
| ndc | product | 84324-033 | openfda.product_ndc |
| ndc11 | package | 84324003301 | derived:openfda.package_ndc |
| rxcui | 251292 | openfda.rxcui | |
| spl id | caaad95a-c75a-4269-9d46-55a55d9353e6 | id | |
| spl set id | a2a3b83f-2d49-4bc4-90d7-1f2a7f4ea45f | 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.