warnings
Warnings Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Opalescence Whitening
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
- Opalescence Whitening
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Ultradent Products, Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d07f842e-b6f1-4ae1-b576-f542ecd02dd4
- SPL ID
- 5b14d90f-23ec-372b-e063-6294a90a2066
- Version
- 10
- Effective date
- 2026-09-09
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:49
| 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 | Opalescence Whitening | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Ultradent Products, Inc | openfda.manufacturer_name | |
| ndc | package | 51206-302-11 | openfda.package_ndc |
| ndc | package | 51206-302-06 | openfda.package_ndc |
| ndc | package | 51206-302-08 | openfda.package_ndc |
| ndc | package | 51206-302-10 | openfda.package_ndc |
| ndc | package | 51206-302-09 | openfda.package_ndc |
| ndc | package | 51206-302-07 | openfda.package_ndc |
| ndc | product | 51206-302 | openfda.product_ndc |
| ndc11 | package | 51206030211 | derived:openfda.package_ndc |
| ndc11 | package | 51206030209 | derived:openfda.package_ndc |
| ndc11 | package | 51206030206 | derived:openfda.package_ndc |
| ndc11 | package | 51206030207 | derived:openfda.package_ndc |
| ndc11 | package | 51206030210 | derived:openfda.package_ndc |
| ndc11 | package | 51206030208 | derived:openfda.package_ndc |
| rxcui | 1044547 | openfda.rxcui | |
| spl id | 5b14d90f-23ec-372b-e063-6294a90a2066 | id | |
| spl set id | d07f842e-b6f1-4ae1-b576-f542ecd02dd4 | 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.