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 Advanced Radiant Mint with Stain Blasting Foam
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 Radiant Mint with Stain Blasting Foam
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4ee26a82-16fd-f0fb-e063-6394a90a91d1
- SPL ID
- 4f09758e-2849-edf1-e063-6394a90a62e8
- Version
- 3
- Effective date
- 2026-04-09
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:29:08
| 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 Advanced Radiant Mint with Stain Blasting Foam | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 84126-629-33 | openfda.package_ndc |
| ndc | package | 84126-629-85 | openfda.package_ndc |
| ndc | package | 84126-629-23 | openfda.package_ndc |
| ndc | package | 84126-629-02 | openfda.package_ndc |
| ndc | package | 84126-629-24 | openfda.package_ndc |
| ndc | package | 84126-629-49 | openfda.package_ndc |
| ndc | package | 84126-629-93 | openfda.package_ndc |
| ndc | product | 84126-629 | openfda.product_ndc |
| ndc11 | package | 84126062933 | derived:openfda.package_ndc |
| ndc11 | package | 84126062923 | derived:openfda.package_ndc |
| ndc11 | package | 84126062924 | derived:openfda.package_ndc |
| ndc11 | package | 84126062985 | derived:openfda.package_ndc |
| ndc11 | package | 84126062949 | derived:openfda.package_ndc |
| ndc11 | package | 84126062993 | derived:openfda.package_ndc |
| ndc11 | package | 84126062902 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 4f09758e-2849-edf1-e063-6394a90a62e8 | id | |
| spl set id | 4ee26a82-16fd-f0fb-e063-6394a90a91d1 | 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.