Crest 3D White Brilliance Advanced Whitening Fresh Mint
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 Advanced Whitening Fresh Mint
- Generic name
- SODIUM MONOFLUOROPHOSPHATE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c8350ab3-9347-58c0-e053-2995a90a7238
- SPL ID
- 47e4eb05-5672-efc0-e063-6294a90a66e0
- Version
- 9
- Effective date
- 2026-01-08
- Source export date
- 2026-11-06
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:45:15
| 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 Brilliance Advanced Whitening Fresh Mint | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 69423-959-03 | openfda.package_ndc |
| ndc | package | 69423-959-30 | openfda.package_ndc |
| ndc | package | 69423-959-38 | openfda.package_ndc |
| ndc | product | 69423-959 | openfda.product_ndc |
| ndc11 | package | 69423095938 | derived:openfda.package_ndc |
| ndc11 | package | 69423095930 | derived:openfda.package_ndc |
| ndc11 | package | 69423095903 | derived:openfda.package_ndc |
| rxcui | 1038995 | openfda.rxcui | |
| spl id | 47e4eb05-5672-efc0-e063-6294a90a66e0 | id | |
| spl set id | c8350ab3-9347-58c0-e053-2995a90a7238 | set_id | |
| unii | C810JCZ56Q | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.