Crest 3D White Advanced
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 Advanced
- Generic name
- SODIUM MONOFLUOROPHOSPHATE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f3aa9a59-b4d4-05d9-e053-2995a90a0aea
- SPL ID
- 47e28597-136d-217d-e063-6294a90a2cec
- Version
- 6
- Effective date
- 2026-01-08
- 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 05:25:47
| 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 | M022 | openfda.application_number | |
| brand name | Crest 3D White Advanced | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 69423-752-30 | openfda.package_ndc |
| ndc | package | 69423-752-23 | openfda.package_ndc |
| ndc | product | 69423-752 | openfda.product_ndc |
| ndc11 | package | 69423075223 | derived:openfda.package_ndc |
| ndc11 | package | 69423075230 | derived:openfda.package_ndc |
| rxcui | 1038995 | openfda.rxcui | |
| spl id | 47e28597-136d-217d-e063-6294a90a2cec | id | |
| spl set id | f3aa9a59-b4d4-05d9-e053-2995a90a0aea | set_id | |
| unii | C810JCZ56Q | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.