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 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 Charcoal
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Procter & Gamble Manfuacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 96247083-39e9-7ca7-e053-2995a90a75d0
- SPL ID
- 47e2ff33-29d9-6dd9-e063-6394a90a5387
- Version
- 10
- Effective date
- 2026-01-08
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:56
| 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 Charcoal | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Procter & Gamble Manfuacturing Company | openfda.manufacturer_name | |
| ndc | package | 37000-945-76 | openfda.package_ndc |
| ndc | package | 37000-945-03 | openfda.package_ndc |
| ndc | package | 37000-945-27 | openfda.package_ndc |
| ndc | package | 37000-945-82 | openfda.package_ndc |
| ndc | package | 37000-945-38 | openfda.package_ndc |
| ndc | package | 37000-945-30 | openfda.package_ndc |
| ndc | package | 37000-945-02 | openfda.package_ndc |
| ndc | package | 37000-945-41 | openfda.package_ndc |
| ndc | product | 37000-945 | openfda.product_ndc |
| ndc11 | package | 37000094541 | derived:openfda.package_ndc |
| ndc11 | package | 37000094503 | derived:openfda.package_ndc |
| ndc11 | package | 37000094530 | derived:openfda.package_ndc |
| ndc11 | package | 37000094538 | derived:openfda.package_ndc |
| ndc11 | package | 37000094576 | derived:openfda.package_ndc |
| ndc11 | package | 37000094582 | derived:openfda.package_ndc |
| ndc11 | package | 37000094502 | derived:openfda.package_ndc |
| ndc11 | package | 37000094527 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 47e2ff33-29d9-6dd9-e063-6394a90a5387 | id | |
| spl set id | 96247083-39e9-7ca7-e053-2995a90a75d0 | 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.