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 Plus Scope plus Whitening Minty Fresh with Mouthwash striped
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 Plus Scope plus Whitening Minty Fresh with Mouthwash striped
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 56091601-74dd-0a3b-e063-6394a90af476
- SPL ID
- 5609b7f5-e667-8fad-e063-6394a90a3cef
- Version
- 2
- Effective date
- 2026-07-07
- 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 06:18:51
| 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 Plus Scope plus Whitening Minty Fresh with Mouthwash striped | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 84126-669-85 | openfda.package_ndc |
| ndc | package | 84126-669-02 | openfda.package_ndc |
| ndc | package | 84126-669-24 | openfda.package_ndc |
| ndc | package | 84126-669-54 | openfda.package_ndc |
| ndc | package | 84126-669-27 | openfda.package_ndc |
| ndc | package | 84126-669-04 | openfda.package_ndc |
| ndc | package | 84126-669-03 | openfda.package_ndc |
| ndc | product | 84126-669 | openfda.product_ndc |
| ndc11 | package | 84126066954 | derived:openfda.package_ndc |
| ndc11 | package | 84126066924 | derived:openfda.package_ndc |
| ndc11 | package | 84126066902 | derived:openfda.package_ndc |
| ndc11 | package | 84126066927 | derived:openfda.package_ndc |
| ndc11 | package | 84126066985 | derived:openfda.package_ndc |
| ndc11 | package | 84126066903 | derived:openfda.package_ndc |
| ndc11 | package | 84126066904 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 5609b7f5-e667-8fad-e063-6394a90a3cef | id | |
| spl set id | 56091601-74dd-0a3b-e063-6394a90af476 | 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.