warnings
Warning 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 3D White Brilliance
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 Brilliance
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 8e189fbd-5094-4398-b96c-8f95d89b9cdd
- SPL ID
- 47e49f8f-fd96-9aa4-e063-6294a90a5e29
- Version
- 21
- Effective date
- 2026-01-08
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:35:07
| 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 3D White Brilliance | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 37000-873-39 | openfda.package_ndc |
| ndc | package | 37000-873-85 | openfda.package_ndc |
| ndc | package | 37000-873-34 | openfda.package_ndc |
| ndc | package | 37000-873-23 | openfda.package_ndc |
| ndc | package | 37000-873-12 | openfda.package_ndc |
| ndc | package | 37000-873-08 | openfda.package_ndc |
| ndc | package | 37000-873-27 | openfda.package_ndc |
| ndc | package | 37000-873-35 | openfda.package_ndc |
| ndc | package | 37000-873-46 | openfda.package_ndc |
| ndc | package | 37000-873-24 | openfda.package_ndc |
| ndc | package | 37000-873-52 | openfda.package_ndc |
| ndc | package | 37000-873-04 | openfda.package_ndc |
| ndc | package | 37000-873-78 | openfda.package_ndc |
| ndc | package | 37000-873-93 | openfda.package_ndc |
| ndc | package | 37000-873-42 | openfda.package_ndc |
| ndc | product | 37000-873 | openfda.product_ndc |
| ndc11 | package | 37000087346 | derived:openfda.package_ndc |
| ndc11 | package | 37000087335 | derived:openfda.package_ndc |
| ndc11 | package | 37000087378 | derived:openfda.package_ndc |
| ndc11 | package | 37000087342 | derived:openfda.package_ndc |
| ndc11 | package | 37000087339 | derived:openfda.package_ndc |
| ndc11 | package | 37000087324 | derived:openfda.package_ndc |
| ndc11 | package | 37000087352 | derived:openfda.package_ndc |
| ndc11 | package | 37000087312 | derived:openfda.package_ndc |
| ndc11 | package | 37000087385 | derived:openfda.package_ndc |
| ndc11 | package | 37000087304 | derived:openfda.package_ndc |
| ndc11 | package | 37000087327 | derived:openfda.package_ndc |
| ndc11 | package | 37000087323 | derived:openfda.package_ndc |
| ndc11 | package | 37000087308 | derived:openfda.package_ndc |
| ndc11 | package | 37000087334 | derived:openfda.package_ndc |
| ndc11 | package | 37000087393 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 47e49f8f-fd96-9aa4-e063-6294a90a5e29 | id | |
| spl set id | 8e189fbd-5094-4398-b96c-8f95d89b9cdd | 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.