warnings
Warnings For rectal use only. Drug Interaction Precaution: Do not take this product if you are presently taking mineral oil, unless directed by a doctor.
ENEMEEZ
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
- ENEMEEZ
- Generic name
- DOCUSATE SODIUM
- Manufacturer
- Quest Products, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0b06445d-0839-497e-bdff-e0fe224a7738
- SPL ID
- 557bfedd-1dff-a1ff-e063-6294a90ad7bc
- Version
- 20
- Effective date
- 2026-06-30
- Source export date
- 2026-10-30
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:19:54
| Harmonized routes |
|---|
| RECTAL |
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 | ENEMEEZ | openfda.brand_name | |
| generic name | DOCUSATE SODIUM | openfda.generic_name | |
| manufacturer name | Quest Products, LLC | openfda.manufacturer_name | |
| ndc | package | 17433-9876-4 | openfda.package_ndc |
| ndc | package | 17433-9876-0 | openfda.package_ndc |
| ndc | package | 17433-9876-3 | openfda.package_ndc |
| ndc | package | 17433-9876-2 | openfda.package_ndc |
| ndc | package | 17433-9876-9 | openfda.package_ndc |
| ndc | package | 17433-9876-1 | openfda.package_ndc |
| ndc | package | 17433-9876-6 | openfda.package_ndc |
| ndc | package | 17433-9876-5 | openfda.package_ndc |
| ndc | product | 17433-9876 | openfda.product_ndc |
| ndc11 | package | 17433987604 | derived:openfda.package_ndc |
| ndc11 | package | 17433987603 | derived:openfda.package_ndc |
| ndc11 | package | 17433987600 | derived:openfda.package_ndc |
| ndc11 | package | 17433987606 | derived:openfda.package_ndc |
| ndc11 | package | 17433987601 | derived:openfda.package_ndc |
| ndc11 | package | 17433987609 | derived:openfda.package_ndc |
| ndc11 | package | 17433987602 | derived:openfda.package_ndc |
| ndc11 | package | 17433987605 | derived:openfda.package_ndc |
| rxcui | 1192923 | openfda.rxcui | |
| rxcui | 1190184 | openfda.rxcui | |
| spl id | 557bfedd-1dff-a1ff-e063-6294a90ad7bc | id | |
| spl set id | 0b06445d-0839-497e-bdff-e0fe224a7738 | 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.