warnings
WARNINGS FOR TOPICAL INTRAORAL USE ONLY. FOR PROFESSIONAL OFFICE USE ONLY. THIS PRODUCT IS NOT INTENDED FOR HOME OR UNSUPERVISED CONSUMER USE.
CURODONT REPAIR FLUORIDE PLUS
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
- CURODONT REPAIR FLUORIDE PLUS
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- CREDENTIS AG
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 03ec09f9-4281-9ccb-e063-6294a90aadd8
- SPL ID
- 28421f54-862e-60e1-e063-6294a90a4af4
- Version
- 3
- Effective date
- 2024-12-01
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:24:34
| 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 |
|---|---|---|---|
| application number | M021 | openfda.application_number | |
| brand name | CURODONT REPAIR FLUORIDE PLUS | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | CREDENTIS AG | openfda.manufacturer_name | |
| ndc | package | 72247-109-12 | openfda.package_ndc |
| ndc | product | 72247-109 | openfda.product_ndc |
| ndc11 | package | 72247010912 | derived:openfda.package_ndc |
| spl id | 28421f54-862e-60e1-e063-6294a90a4af4 | id | |
| spl set id | 03ec09f9-4281-9ccb-e063-6294a90aadd8 | set_id | |
| unii | 8ZYQ1474W7 | 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.