warnings
Warning 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.
Crest 3D White Luxe Diamond Strong
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 3D White Luxe Diamond Strong
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c1420129-5460-4900-ac9a-356d2d7c60a2
- SPL ID
- 48ea8786-3ce3-a637-e063-6294a90ab4a9
- Version
- 11
- Effective date
- 2026-01-21
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:27:24
| 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 | Crest 3D White Luxe Diamond Strong | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 37000-862-01 | openfda.package_ndc |
| ndc | package | 37000-862-03 | openfda.package_ndc |
| ndc | package | 37000-862-02 | openfda.package_ndc |
| ndc | product | 37000-862 | openfda.product_ndc |
| ndc11 | package | 37000086201 | derived:openfda.package_ndc |
| ndc11 | package | 37000086202 | derived:openfda.package_ndc |
| ndc11 | package | 37000086203 | derived:openfda.package_ndc |
| rxcui | 1486338 | openfda.rxcui | |
| rxcui | 1090579 | openfda.rxcui | |
| spl id | 48ea8786-3ce3-a637-e063-6294a90ab4a9 | id | |
| spl set id | c1420129-5460-4900-ac9a-356d2d7c60a2 | 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.