FDA label 326baeb1-1aab-416a-e063-6294a90a257c
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
- ac4edf64-6e56-57f3-e053-2a95a90ae7a8
- SPL ID
- 326baeb1-1aab-416a-e063-6294a90a257c
- Version
- 5
- Effective date
- 2025-04-10
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:58:20
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 | 326baeb1-1aab-416a-e063-6294a90a257c | id | |
| spl set id | ac4edf64-6e56-57f3-e053-2a95a90ae7a8 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings Ask a doctor or pharmacist before use if you are lactose-intolerant. Stop use and ask a doctor if symptoms persist or worsen. If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. A llergic (hypersensitivity) reactions may occur i n very rare cases. Do not use if known sensitivity to Brillia Health Cold-Flu Recovery or any of its ingredients exists.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Allergic Reaction Allergic (hypersensitivity) reactions may occur i n very rare cases.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.