warnings
label warnings
FDA label f1f0ab04-0096-9db4-e053-2995a90aa04c
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
- SPL set ID
- b8434772-26c8-fce9-e053-2995a90abc7c
- SPL ID
- f1f0ab04-0096-9db4-e053-2995a90aa04c
- Version
- 2
- Effective date
- 2023-01-10
- Source export date
- 2026-11-06
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:11:52
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 |
|---|---|---|---|
| spl id | f1f0ab04-0096-9db4-e053-2995a90aa04c | id | |
| spl set id | b8434772-26c8-fce9-e053-2995a90abc7c | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
These highlights do not include all the information needed to use. See full prescribing information for Lactulose Initial U.S. Approval. To report suspected adverse reactions contact lannet Company Inc at 1-800-332-1088 Label Adverse Reactions
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.