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 Premium Plus Scope Dual Blast Active 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 Premium Plus Scope Dual Blast Active Foam
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b788d16a-8a58-0352-e053-2a95a90a965e
- SPL ID
- 47e3398c-efdd-b995-e063-6394a90a2a9b
- Version
- 13
- Effective date
- 2026-01-08
- 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 06:17:12
| 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 Premium Plus Scope Dual Blast Active Foam | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 37000-990-72 | openfda.package_ndc |
| ndc | package | 37000-990-35 | openfda.package_ndc |
| ndc | package | 37000-990-03 | openfda.package_ndc |
| ndc | package | 37000-990-23 | openfda.package_ndc |
| ndc | package | 37000-990-52 | openfda.package_ndc |
| ndc | product | 37000-990 | openfda.product_ndc |
| ndc11 | package | 37000099052 | derived:openfda.package_ndc |
| ndc11 | package | 37000099072 | derived:openfda.package_ndc |
| ndc11 | package | 37000099003 | derived:openfda.package_ndc |
| ndc11 | package | 37000099035 | derived:openfda.package_ndc |
| ndc11 | package | 37000099023 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 47e3398c-efdd-b995-e063-6394a90a2a9b | id | |
| spl set id | b788d16a-8a58-0352-e053-2a95a90a965e | 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.