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 Complete Multi-Benefit Whitening plus Scope
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 Complete Multi-Benefit Whitening plus Scope
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Procter & Gamble Manufactura, S. de R.L. de C.V.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0206710a-707f-4aa9-96b9-86240c1275dc
- SPL ID
- 508aa851-a857-c4a4-e063-6294a90aedf6
- Version
- 13
- Effective date
- 2026-04-28
- 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 06:29:05
| 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 Complete Multi-Benefit Whitening plus Scope | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Procter & Gamble Manufactura, S. de R.L. de C.V. | openfda.manufacturer_name | |
| ndc | package | 58933-020-54 | openfda.package_ndc |
| ndc | package | 58933-020-08 | openfda.package_ndc |
| ndc | package | 58933-020-01 | openfda.package_ndc |
| ndc | package | 58933-020-03 | openfda.package_ndc |
| ndc | package | 58933-020-85 | openfda.package_ndc |
| ndc | package | 58933-020-06 | openfda.package_ndc |
| ndc | product | 58933-020 | openfda.product_ndc |
| ndc11 | package | 58933002008 | derived:openfda.package_ndc |
| ndc11 | package | 58933002054 | derived:openfda.package_ndc |
| ndc11 | package | 58933002085 | derived:openfda.package_ndc |
| ndc11 | package | 58933002006 | derived:openfda.package_ndc |
| ndc11 | package | 58933002001 | derived:openfda.package_ndc |
| ndc11 | package | 58933002003 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 508aa851-a857-c4a4-e063-6294a90aedf6 | id | |
| spl set id | 0206710a-707f-4aa9-96b9-86240c1275dc | 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.