warnings
Warnings Do not use if irritation occurs and persists.
Advance White Extreme Whitening Tartar Control
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
- Advance White Extreme Whitening Tartar Control
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Church & Dwight Co., Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b539264f-e1ff-440b-af76-84266fe2c0a2
- SPL ID
- 44fa11f4-4ddd-e970-e063-6394a90a307e
- Version
- 13
- Effective date
- 2025-12-02
- Source export date
- 2026-10-27
- 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/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:44:51
| 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 | Advance White Extreme Whitening Tartar Control | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Church & Dwight Co., Inc. | openfda.manufacturer_name | |
| ndc | package | 10237-658-09 | openfda.package_ndc |
| ndc | package | 10237-658-72 | openfda.package_ndc |
| ndc | package | 10237-658-60 | openfda.package_ndc |
| ndc | package | 10237-658-28 | openfda.package_ndc |
| ndc | package | 10237-658-43 | openfda.package_ndc |
| ndc | package | 10237-658-46 | openfda.package_ndc |
| ndc | package | 10237-658-12 | openfda.package_ndc |
| ndc | product | 10237-658 | openfda.product_ndc |
| ndc11 | package | 10237065846 | derived:openfda.package_ndc |
| ndc11 | package | 10237065860 | derived:openfda.package_ndc |
| ndc11 | package | 10237065828 | derived:openfda.package_ndc |
| ndc11 | package | 10237065872 | derived:openfda.package_ndc |
| ndc11 | package | 10237065843 | derived:openfda.package_ndc |
| ndc11 | package | 10237065809 | derived:openfda.package_ndc |
| ndc11 | package | 10237065812 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | 44fa11f4-4ddd-e970-e063-6394a90a307e | id | |
| spl set id | b539264f-e1ff-440b-af76-84266fe2c0a2 | 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.