warnings
Warnings Keep out of the reach of children. If more than used for rinsing is accidentally swallowed, gel medical help or contact a Poison Control Center right away. Do not use with another fluoride rinse on the same day.
Therabreath Overnight Chamomile Mint
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 Overnight Chamomile Mint
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Church & Dwight Co., Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cc0c533c-145e-4877-b421-1baf3a3a572e
- SPL ID
- 45a8183b-aa06-ed02-e063-6394a90a46f5
- Version
- 4
- Effective date
- 2025-12-11
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:54:47
| 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 Overnight Chamomile Mint | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Church & Dwight Co., Inc. | openfda.manufacturer_name | |
| ndc | package | 10237-262-26 | openfda.package_ndc |
| ndc | package | 10237-262-16 | openfda.package_ndc |
| ndc | product | 10237-262 | openfda.product_ndc |
| ndc11 | package | 10237026216 | derived:openfda.package_ndc |
| ndc11 | package | 10237026226 | derived:openfda.package_ndc |
| rxcui | 240698 | openfda.rxcui | |
| spl id | 45a8183b-aa06-ed02-e063-6394a90a46f5 | id | |
| spl set id | cc0c533c-145e-4877-b421-1baf3a3a572e | 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.