warnings
Warnings Keep out of reach of children under 6 yrs. of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Crest Cavity Protection Cool Mint Gel
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
- Crest Cavity Protection Cool Mint Gel
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 102e4d9c-0fae-d48a-e063-6294a90aac94
- SPL ID
- 49ef9a5d-2bd1-2d93-e063-6394a90a3fe3
- Version
- 10
- Effective date
- 2026-02-03
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:58
| 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 | Crest Cavity Protection Cool Mint Gel | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 69423-815-24 | openfda.package_ndc |
| ndc | package | 69423-815-42 | openfda.package_ndc |
| ndc | package | 69423-815-35 | openfda.package_ndc |
| ndc | package | 69423-815-82 | openfda.package_ndc |
| ndc | package | 69423-815-57 | openfda.package_ndc |
| ndc | package | 69423-815-85 | openfda.package_ndc |
| ndc | package | 69423-815-11 | openfda.package_ndc |
| ndc | product | 69423-815 | openfda.product_ndc |
| ndc11 | package | 69423081542 | derived:openfda.package_ndc |
| ndc11 | package | 69423081535 | derived:openfda.package_ndc |
| ndc11 | package | 69423081582 | derived:openfda.package_ndc |
| ndc11 | package | 69423081557 | derived:openfda.package_ndc |
| ndc11 | package | 69423081511 | derived:openfda.package_ndc |
| ndc11 | package | 69423081524 | derived:openfda.package_ndc |
| ndc11 | package | 69423081585 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 49ef9a5d-2bd1-2d93-e063-6394a90a3fe3 | id | |
| spl set id | 102e4d9c-0fae-d48a-e063-6294a90aac94 | 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.