warnings
Warnings • Keep out of reach of children under 6 years of age. • If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
DENTI BUONGIORNO GUM CARE COOL MINT TOOTH
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
- DENTI BUONGIORNO GUM CARE COOL MINT TOOTH
- Generic name
- SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE
- Manufacturer
- DONG IL PHARMS CO.,LTD
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 487d689d-ebdd-43c3-e063-6294a90af0e2
- SPL ID
- 487d73be-0ff9-f417-e063-6394a90a0668
- Version
- 1
- Effective date
- 2026-01-16
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:21
| 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 | DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | openfda.brand_name | |
| generic name | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | openfda.generic_name | |
| manufacturer name | DONG IL PHARMS CO.,LTD | openfda.manufacturer_name | |
| ndc | package | 73242-1127-2 | openfda.package_ndc |
| ndc | package | 73242-1127-1 | openfda.package_ndc |
| ndc | product | 73242-1127 | openfda.product_ndc |
| ndc11 | package | 73242112701 | derived:openfda.package_ndc |
| ndc11 | package | 73242112702 | derived:openfda.package_ndc |
| rxcui | 2713755 | openfda.rxcui | |
| spl id | 487d73be-0ff9-f417-e063-6394a90a0668 | id | |
| spl set id | 487d689d-ebdd-43c3-e063-6294a90af0e2 | set_id | |
| unii | 8ZYQ1474W7 | openfda.unii | |
| unii | ETJ7Z6XBU4 | openfda.unii | |
| unii | 9E8X80D2L0 | 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.