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 Arctic Fresh
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 Arctic Fresh
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- fa08a877-b9e5-4eba-b832-3a28f4f3f83c
- SPL ID
- 4ee301a4-a350-8e4c-e063-6394a90a2263
- Version
- 22
- Effective date
- 2026-04-07
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:17:36
| Harmonized routes |
|---|
| DENTAL, 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 Arctic Fresh | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 37000-875-49 | openfda.package_ndc |
| ndc | package | 37000-875-64 | openfda.package_ndc |
| ndc | package | 37000-875-56 | openfda.package_ndc |
| ndc | package | 37000-875-27 | openfda.package_ndc |
| ndc | package | 37000-875-08 | openfda.package_ndc |
| ndc | package | 37000-875-77 | openfda.package_ndc |
| ndc | package | 37000-875-24 | openfda.package_ndc |
| ndc | package | 37000-875-29 | openfda.package_ndc |
| ndc | package | 37000-875-30 | openfda.package_ndc |
| ndc | package | 37000-875-99 | openfda.package_ndc |
| ndc | package | 37000-875-15 | openfda.package_ndc |
| ndc | package | 37000-875-63 | openfda.package_ndc |
| ndc | package | 37000-875-42 | openfda.package_ndc |
| ndc | package | 37000-875-07 | openfda.package_ndc |
| ndc | package | 37000-875-13 | openfda.package_ndc |
| ndc | package | 37000-875-93 | openfda.package_ndc |
| ndc | package | 37000-875-06 | openfda.package_ndc |
| ndc | package | 37000-875-50 | openfda.package_ndc |
| ndc | package | 37000-875-02 | openfda.package_ndc |
| ndc | package | 37000-875-03 | openfda.package_ndc |
| ndc | package | 37000-875-54 | openfda.package_ndc |
| ndc | package | 37000-875-04 | openfda.package_ndc |
| ndc | package | 37000-875-41 | openfda.package_ndc |
| ndc | package | 37000-875-38 | openfda.package_ndc |
| ndc | package | 37000-875-10 | openfda.package_ndc |
| ndc | package | 37000-875-33 | openfda.package_ndc |
| ndc | product | 37000-875 | openfda.product_ndc |
| ndc11 | package | 37000087515 | derived:openfda.package_ndc |
| ndc11 | package | 37000087506 | derived:openfda.package_ndc |
| ndc11 | package | 37000087538 | derived:openfda.package_ndc |
| ndc11 | package | 37000087510 | derived:openfda.package_ndc |
| ndc11 | package | 37000087542 | derived:openfda.package_ndc |
| ndc11 | package | 37000087530 | derived:openfda.package_ndc |
| ndc11 | package | 37000087502 | derived:openfda.package_ndc |
| ndc11 | package | 37000087533 | derived:openfda.package_ndc |
| ndc11 | package | 37000087508 | derived:openfda.package_ndc |
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.