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 Active Foam plus Whitening Minty 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 Premium Plus Scope Active Foam plus Whitening Minty Fresh
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 560815d6-018a-0c24-e063-6394a90a1071
- SPL ID
- 560826ac-ae5b-1c37-e063-6394a90af9ea
- Version
- 1
- Effective date
- 2026-07-07
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:48:52
| 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 Active Foam plus Whitening Minty Fresh | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 84126-668-03 | openfda.package_ndc |
| ndc | package | 84126-668-52 | openfda.package_ndc |
| ndc | package | 84126-668-04 | openfda.package_ndc |
| ndc | product | 84126-668 | openfda.product_ndc |
| ndc11 | package | 84126066852 | derived:openfda.package_ndc |
| ndc11 | package | 84126066804 | derived:openfda.package_ndc |
| ndc11 | package | 84126066803 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 560826ac-ae5b-1c37-e063-6394a90af9ea | id | |
| spl set id | 560815d6-018a-0c24-e063-6394a90a1071 | 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.