warnings
Warnings Do not use if irritation occurs and persists. 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.
A and H Plus Therabreath Breath Freshners
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
- A and H Plus Therabreath Breath Freshners
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Church & Dwight Co., Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 18d6073e-b1ee-47d2-9758-2cf04f3cf3ca
- SPL ID
- 501aaf53-e8df-0380-e063-6394a90aca25
- Version
- 9
- Effective date
- 2026-04-23
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:17:40
| 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 | A and H Plus Therabreath Breath Freshners | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Church & Dwight Co., Inc. | openfda.manufacturer_name | |
| ndc | package | 10237-676-56 | openfda.package_ndc |
| ndc | package | 10237-676-51 | openfda.package_ndc |
| ndc | package | 10237-676-45 | openfda.package_ndc |
| ndc | package | 10237-676-09 | openfda.package_ndc |
| ndc | package | 10237-676-55 | openfda.package_ndc |
| ndc | product | 10237-676 | openfda.product_ndc |
| ndc11 | package | 10237067655 | derived:openfda.package_ndc |
| ndc11 | package | 10237067651 | derived:openfda.package_ndc |
| ndc11 | package | 10237067656 | derived:openfda.package_ndc |
| ndc11 | package | 10237067645 | derived:openfda.package_ndc |
| ndc11 | package | 10237067609 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | 501aaf53-e8df-0380-e063-6394a90aca25 | id | |
| spl set id | 18d6073e-b1ee-47d2-9758-2cf04f3cf3ca | 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.