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 Active Foam Whitening 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 Premium Plus Active Foam Whitening scope
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 55004d9d-eda7-a285-e063-6294a90ad4ca
- SPL ID
- 55003edd-9f63-d73e-e063-6394a90a05c6
- Version
- 1
- Effective date
- 2026-06-24
- Source export date
- 2026-10-27
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:15:08
| 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 Premium Plus Active Foam Whitening scope | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | The Procter & Gamble Manufacturing Company | openfda.manufacturer_name | |
| ndc | package | 84126-660-72 | openfda.package_ndc |
| ndc | package | 84126-660-03 | openfda.package_ndc |
| ndc | package | 84126-660-52 | openfda.package_ndc |
| ndc | product | 84126-660 | openfda.product_ndc |
| ndc11 | package | 84126066003 | derived:openfda.package_ndc |
| ndc11 | package | 84126066072 | derived:openfda.package_ndc |
| ndc11 | package | 84126066052 | derived:openfda.package_ndc |
| rxcui | 891775 | openfda.rxcui | |
| spl id | 55003edd-9f63-d73e-e063-6394a90a05c6 | id | |
| spl set id | 55004d9d-eda7-a285-e063-6294a90ad4ca | 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.