warnings
Warnings Keep out of the 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 immediately.
Nature Mint 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
- Nature Mint Anticavity
- Generic name
- SODIUM MONOFLUOROPHOSPHATE
- Manufacturer
- Bob Barker Company Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 916891d3-5234-46a8-a492-21a31f36a852
- SPL ID
- 55d17227-845f-4c84-a5f1-cae38db6f024
- Version
- 1
- Effective date
- 2024-02-02
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:07:44
| Harmonized routes |
|---|
| DENTAL |
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 | Nature Mint Anticavity | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE | openfda.generic_name | |
| manufacturer name | Bob Barker Company Inc. | openfda.manufacturer_name | |
| ndc | package | 53247-129-02 | openfda.package_ndc |
| ndc | package | 53247-129-07 | openfda.package_ndc |
| ndc | package | 53247-129-06 | openfda.package_ndc |
| ndc | package | 53247-129-01 | openfda.package_ndc |
| ndc | package | 53247-129-03 | openfda.package_ndc |
| ndc | package | 53247-129-05 | openfda.package_ndc |
| ndc | package | 53247-129-04 | openfda.package_ndc |
| ndc | product | 53247-129 | openfda.product_ndc |
| ndc11 | package | 53247012907 | derived:openfda.package_ndc |
| ndc11 | package | 53247012906 | derived:openfda.package_ndc |
| ndc11 | package | 53247012905 | derived:openfda.package_ndc |
| ndc11 | package | 53247012902 | derived:openfda.package_ndc |
| ndc11 | package | 53247012904 | derived:openfda.package_ndc |
| ndc11 | package | 53247012901 | derived:openfda.package_ndc |
| ndc11 | package | 53247012903 | derived:openfda.package_ndc |
| rxcui | 545626 | openfda.rxcui | |
| spl id | 55d17227-845f-4c84-a5f1-cae38db6f024 | id | |
| spl set id | 916891d3-5234-46a8-a492-21a31f36a852 | set_id | |
| unii | C810JCZ56Q | 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.