warnings and cautions
Warnings Do not use if you are presently taking mineral oil, unless told todo so by a doctor
Colace
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
- Colace
- Generic name
- DOCUSATE SODIUM
- Manufacturer
- Atlantis Consumer Healthcare, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7793fced-e8ee-44e2-b212-dd2a59a5f462
- SPL ID
- 650714ee-2cec-42c9-8631-b3f8ebc7348f
- Version
- 18
- Effective date
- 2026-08-04
- 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 05:56:12
| 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 | Colace | openfda.brand_name | |
| generic name | DOCUSATE SODIUM | openfda.generic_name | |
| manufacturer name | Atlantis Consumer Healthcare, Inc. | openfda.manufacturer_name | |
| ndc | package | 67618-101-25 | openfda.package_ndc |
| ndc | package | 67618-101-60 | openfda.package_ndc |
| ndc | package | 67618-101-30 | openfda.package_ndc |
| ndc | package | 67618-101-51 | openfda.package_ndc |
| ndc | package | 67618-101-01 | openfda.package_ndc |
| ndc | package | 67618-101-10 | openfda.package_ndc |
| ndc | package | 67618-101-52 | openfda.package_ndc |
| ndc | product | 67618-101 | openfda.product_ndc |
| ndc11 | package | 67618010152 | derived:openfda.package_ndc |
| ndc11 | package | 67618010101 | derived:openfda.package_ndc |
| ndc11 | package | 67618010130 | derived:openfda.package_ndc |
| ndc11 | package | 67618010125 | derived:openfda.package_ndc |
| ndc11 | package | 67618010110 | derived:openfda.package_ndc |
| ndc11 | package | 67618010160 | derived:openfda.package_ndc |
| ndc11 | package | 67618010151 | derived:openfda.package_ndc |
| rxcui | 1247756 | openfda.rxcui | |
| rxcui | 1115005 | openfda.rxcui | |
| spl id | 650714ee-2cec-42c9-8631-b3f8ebc7348f | id | |
| spl set id | 7793fced-e8ee-44e2-b212-dd2a59a5f462 | 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.