warnings
Warnings Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Listerine Total Care Fresh Mint Anticavity Fluoride
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
- Listerine Total Care Fresh Mint Anticavity Fluoride
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Kenvue Brands LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ed15e0b9-00c9-0df1-e053-2a95a90a42c0
- SPL ID
- 2f34589b-07a1-9fef-e063-6394a90a851a
- Version
- 6
- Effective date
- 2025-02-28
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:04:38
| 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 | Listerine Total Care Fresh Mint Anticavity Fluoride | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Kenvue Brands LLC | openfda.manufacturer_name | |
| ndc | package | 69968-0787-5 | openfda.package_ndc |
| ndc | package | 69968-0787-4 | openfda.package_ndc |
| ndc | package | 69968-0787-3 | openfda.package_ndc |
| ndc | package | 69968-0787-1 | openfda.package_ndc |
| ndc | package | 69968-0787-6 | openfda.package_ndc |
| ndc | package | 69968-0787-2 | openfda.package_ndc |
| ndc | product | 69968-0787 | openfda.product_ndc |
| ndc11 | package | 69968078702 | derived:openfda.package_ndc |
| ndc11 | package | 69968078704 | derived:openfda.package_ndc |
| ndc11 | package | 69968078705 | derived:openfda.package_ndc |
| ndc11 | package | 69968078706 | derived:openfda.package_ndc |
| ndc11 | package | 69968078701 | derived:openfda.package_ndc |
| ndc11 | package | 69968078703 | derived:openfda.package_ndc |
| rxcui | 313029 | openfda.rxcui | |
| rxcui | 1798474 | openfda.rxcui | |
| spl id | 2f34589b-07a1-9fef-e063-6394a90a851a | id | |
| spl set id | ed15e0b9-00c9-0df1-e053-2a95a90a42c0 | 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.