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 3D White Whitening Therapy Deep Clean Charcoal
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 Whitening Therapy Deep Clean Charcoal
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Procter & Gamble Manfuacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 812c1519-1a4b-2495-e053-2a91aa0a914a
- SPL ID
- 4f0acb10-3b14-9742-e063-6294a90ac9da
- Version
- 15
- Effective date
- 2026-04-09
- 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 05:35:56
| 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 Whitening Therapy Deep Clean Charcoal | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Procter & Gamble Manfuacturing Company | openfda.manufacturer_name | |
| ndc | package | 37000-215-04 | openfda.package_ndc |
| ndc | package | 37000-215-60 | openfda.package_ndc |
| ndc | package | 37000-215-28 | openfda.package_ndc |
| ndc | package | 37000-215-52 | openfda.package_ndc |
| ndc | package | 37000-215-46 | openfda.package_ndc |
| ndc | package | 37000-215-05 | openfda.package_ndc |
| ndc | package | 37000-215-92 | openfda.package_ndc |
| ndc | package | 37000-215-35 | openfda.package_ndc |
| ndc | package | 37000-215-24 | openfda.package_ndc |
| ndc | package | 37000-215-03 | openfda.package_ndc |
| ndc | package | 37000-215-85 | openfda.package_ndc |
| ndc | package | 37000-215-82 | openfda.package_ndc |
| ndc | package | 37000-215-08 | openfda.package_ndc |
| ndc | package | 37000-215-41 | openfda.package_ndc |
| ndc | product | 37000-215 | openfda.product_ndc |
| ndc11 | package | 37000021528 | derived:openfda.package_ndc |
| ndc11 | package | 37000021505 | derived:openfda.package_ndc |
| ndc11 | package | 37000021524 | derived:openfda.package_ndc |
| ndc11 | package | 37000021592 | derived:openfda.package_ndc |
| ndc11 | package | 37000021585 | derived:openfda.package_ndc |
| ndc11 | package | 37000021535 | derived:openfda.package_ndc |
| ndc11 | package | 37000021546 | derived:openfda.package_ndc |
| ndc11 | package | 37000021508 | derived:openfda.package_ndc |
| ndc11 | package | 37000021552 | derived:openfda.package_ndc |
| ndc11 | package | 37000021504 | derived:openfda.package_ndc |
| ndc11 | package | 37000021560 | derived:openfda.package_ndc |
| ndc11 | package | 37000021582 | derived:openfda.package_ndc |
| ndc11 | package | 37000021503 | derived:openfda.package_ndc |
| ndc11 | package | 37000021541 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 4f0acb10-3b14-9742-e063-6294a90ac9da | id | |
| spl set id | 812c1519-1a4b-2495-e053-2a91aa0a914a | 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.