warnings
Warnings If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center (1-800-222-1222) immediatley. Keep out of reach of children Keep out of reach of childen under 6 years of age
Sodium Monofluorophosphate
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
- Sodium Monofluorophosphate
- Generic name
- WHITE TOOTHPASTE
- Manufacturer
- Dynarex Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1be422b9-6320-ed5c-e063-6294a90a7e42
- SPL ID
- 1c58c582-92e0-4533-e063-6394a90a9fe5
- Version
- 2
- Effective date
- 2024-07-03
- Source export date
- 2026-09-28
- 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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:16:02
| 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 | Sodium Monofluorophosphate | openfda.brand_name | |
| generic name | WHITE TOOTHPASTE | openfda.generic_name | |
| manufacturer name | Dynarex Corporation | openfda.manufacturer_name | |
| ndc | package | 67777-181-03 | openfda.package_ndc |
| ndc | package | 67777-181-04 | openfda.package_ndc |
| ndc | package | 67777-181-05 | openfda.package_ndc |
| ndc | package | 67777-181-07 | openfda.package_ndc |
| ndc | package | 67777-181-09 | openfda.package_ndc |
| ndc | package | 67777-181-02 | openfda.package_ndc |
| ndc | package | 67777-181-01 | openfda.package_ndc |
| ndc | package | 67777-181-06 | openfda.package_ndc |
| ndc | package | 67777-181-08 | openfda.package_ndc |
| ndc | package | 67777-181-13 | openfda.package_ndc |
| ndc | package | 67777-181-11 | openfda.package_ndc |
| ndc | package | 67777-181-12 | openfda.package_ndc |
| ndc | package | 67777-181-10 | openfda.package_ndc |
| ndc | product | 67777-181 | openfda.product_ndc |
| ndc11 | package | 67777018102 | derived:openfda.package_ndc |
| ndc11 | package | 67777018104 | derived:openfda.package_ndc |
| ndc11 | package | 67777018106 | derived:openfda.package_ndc |
| ndc11 | package | 67777018110 | derived:openfda.package_ndc |
| ndc11 | package | 67777018101 | derived:openfda.package_ndc |
| ndc11 | package | 67777018108 | derived:openfda.package_ndc |
| ndc11 | package | 67777018105 | derived:openfda.package_ndc |
| ndc11 | package | 67777018103 | derived:openfda.package_ndc |
| ndc11 | package | 67777018111 | derived:openfda.package_ndc |
| ndc11 | package | 67777018109 | derived:openfda.package_ndc |
| ndc11 | package | 67777018107 | derived:openfda.package_ndc |
| ndc11 | package | 67777018112 | derived:openfda.package_ndc |
| ndc11 | package | 67777018113 | derived:openfda.package_ndc |
| rxcui | 545626 | openfda.rxcui | |
| spl id | 1c58c582-92e0-4533-e063-6394a90a9fe5 | id | |
| spl set id | 1be422b9-6320-ed5c-e063-6294a90a7e42 | set_id | |
| unii | C810JCZ56Q | 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.