warnings
WARNINGS Stop use and ask a physician if symptoms persist for more than 3 days or worsen.
Calcarea Carbonic 200ck
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
- Calcarea Carbonic 200ck
- Generic name
- OYSTER SHELL CALCIUM CARBONATE, CRUDE
- Manufacturer
- SEVENE USA
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c8d4f3b3-166d-2411-e053-2a95a90abb4a
- SPL ID
- 35b7c0bd-0148-0928-e063-6294a90aad27
- Version
- 5
- Effective date
- 2025-05-22
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:31
| Harmonized routes |
|---|
| SUBLINGUAL |
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 | Calcarea Carbonic 200ck | openfda.brand_name | |
| generic name | OYSTER SHELL CALCIUM CARBONATE, CRUDE | openfda.generic_name | |
| manufacturer name | SEVENE USA | openfda.manufacturer_name | |
| ndc | package | 76472-3008-1 | openfda.package_ndc |
| ndc | product | 76472-3008 | openfda.product_ndc |
| ndc11 | package | 76472300801 | derived:openfda.package_ndc |
| spl id | 35b7c0bd-0148-0928-e063-6294a90aad27 | id | |
| spl set id | c8d4f3b3-166d-2411-e053-2a95a90abb4a | set_id | |
| unii | 2E32821G6I | 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.