warnings
Warnings If pregnant or breast-feeding, consult a health professional before use.
Lithium
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
- Lithium
- Generic name
- LITHIUM BROMATUM
- Manufacturer
- Marco Pharma International LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f4a1d451-33ad-4df3-ae68-58cfbfccfa89
- SPL ID
- 483c1e49-a5da-749f-e063-6394a90a226e
- Version
- 6
- Effective date
- 2026-01-12
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:55
| 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 |
|---|---|---|---|
| brand name | Lithium | openfda.brand_name | |
| generic name | LITHIUM BROMATUM | openfda.generic_name | |
| manufacturer name | Marco Pharma International LLC. | openfda.manufacturer_name | |
| ndc | package | 60986-1019-4 | openfda.package_ndc |
| ndc | package | 60986-1019-3 | openfda.package_ndc |
| ndc | product | 60986-1019 | openfda.product_ndc |
| ndc11 | package | 60986101903 | derived:openfda.package_ndc |
| ndc11 | package | 60986101904 | derived:openfda.package_ndc |
| spl id | 483c1e49-a5da-749f-e063-6394a90a226e | id | |
| spl set id | f4a1d451-33ad-4df3-ae68-58cfbfccfa89 | set_id | |
| unii | 864G646I84 | 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.