warnings
Warnings Do not use: If you are currently taking mineral oil, unless directed by a doctor. When abdominal pain, nausea, or vomiting are present. For longer than one week unless directed by a doctor.
Docusate Sodium
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
- Docusate Sodium
- Generic name
- DOCUSATE SODIUM
- Manufacturer
- AvPAK
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f31a4349-7826-45c0-9388-6b938d167b7a
- SPL ID
- 2b49133c-a8b5-b411-e063-6294a90a3600
- Version
- 9
- Effective date
- 2025-01-09
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:12:41
| 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 | Docusate Sodium | openfda.brand_name | |
| generic name | DOCUSATE SODIUM | openfda.generic_name | |
| manufacturer name | AvPAK | openfda.manufacturer_name | |
| ndc | package | 50268-268-11 | openfda.package_ndc |
| ndc | package | 50268-268-15 | openfda.package_ndc |
| ndc | product | 50268-268 | openfda.product_ndc |
| ndc11 | package | 50268026815 | derived:openfda.package_ndc |
| ndc11 | package | 50268026811 | derived:openfda.package_ndc |
| rxcui | 1245468 | openfda.rxcui | |
| spl id | 2b49133c-a8b5-b411-e063-6294a90a3600 | id | |
| spl set id | f31a4349-7826-45c0-9388-6b938d167b7a | set_id | |
| unii | F05Q2T2JA0 | 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.