Lapis albus
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
- Lapis albus
- Generic name
- CALCIUM HEXAFLUOROSILICATE
- Manufacturer
- Boiron
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 68f897e3-b391-1cca-e053-2a91aa0ae21d
- SPL ID
- 0a0e6b08-3f33-b3f7-e063-6394a90ae8e3
- Version
- 3
- Effective date
- 2023-11-13
- Source export date
- 2026-11-06
- 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/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:50:38
| 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 | Lapis albus | openfda.brand_name | |
| generic name | CALCIUM HEXAFLUOROSILICATE | openfda.generic_name | |
| manufacturer name | Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-3053-41 | openfda.package_ndc |
| ndc | product | 0220-3053 | openfda.product_ndc |
| ndc11 | package | 00220305341 | derived:openfda.package_ndc |
| spl id | 0a0e6b08-3f33-b3f7-e063-6394a90ae8e3 | id | |
| spl set id | 68f897e3-b391-1cca-e053-2a91aa0ae21d | set_id | |
| unii | 2NVP93XVQ3 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.