warnings
Warnings
Laxacin
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
- Laxacin
- Generic name
- DOCUSATE SODIUM AND SENNOSIDES
- Manufacturer
- Alexso, Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0df9abaf-3997-4dde-8003-ae3d8d07cf39
- SPL ID
- 1b45f6d1-4436-4b3a-813b-7043c0d0fad6
- Version
- 8
- Effective date
- 2024-12-04
- Source export date
- 2026-10-12
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:41:12
| 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 | Laxacin | openfda.brand_name | |
| generic name | DOCUSATE SODIUM AND SENNOSIDES | openfda.generic_name | |
| manufacturer name | Alexso, Inc | openfda.manufacturer_name | |
| ndc | package | 50488-0901-1 | openfda.package_ndc |
| ndc | product | 50488-0901 | openfda.product_ndc |
| ndc11 | package | 50488090101 | derived:openfda.package_ndc |
| rxcui | 2106884 | openfda.rxcui | |
| rxcui | 998740 | openfda.rxcui | |
| spl id | 1b45f6d1-4436-4b3a-813b-7043c0d0fad6 | id | |
| spl set id | 0df9abaf-3997-4dde-8003-ae3d8d07cf39 | set_id | |
| unii | F05Q2T2JA0 | openfda.unii | |
| unii | 1B5FPI42EN | 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.