warnings
Warnings Keep out of the reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Therabreath Anticavity
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
- Therabreath Anticavity
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Church & Dwight Co., Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- feab3d45-ff95-4b32-8258-7d932a7380c9
- SPL ID
- 53d7150b-d8de-145c-e063-6394a90ac434
- Version
- 5
- Effective date
- 2026-06-01
- 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 05:12:31
| 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 | Therabreath Anticavity | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Church & Dwight Co., Inc. | openfda.manufacturer_name | |
| ndc | package | 10237-260-20 | openfda.package_ndc |
| ndc | package | 10237-260-01 | openfda.package_ndc |
| ndc | package | 10237-260-16 | openfda.package_ndc |
| ndc | package | 10237-260-03 | openfda.package_ndc |
| ndc | package | 10237-260-10 | openfda.package_ndc |
| ndc | package | 10237-260-26 | openfda.package_ndc |
| ndc | product | 10237-260 | openfda.product_ndc |
| ndc11 | package | 10237026010 | derived:openfda.package_ndc |
| ndc11 | package | 10237026003 | derived:openfda.package_ndc |
| ndc11 | package | 10237026001 | derived:openfda.package_ndc |
| ndc11 | package | 10237026016 | derived:openfda.package_ndc |
| ndc11 | package | 10237026026 | derived:openfda.package_ndc |
| ndc11 | package | 10237026020 | derived:openfda.package_ndc |
| spl id | 53d7150b-d8de-145c-e063-6394a90ac434 | id | |
| spl set id | feab3d45-ff95-4b32-8258-7d932a7380c9 | 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.