warnings
Warning
UNIVERSAL ANTI-CAVITY FLUORIDE
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
- UNIVERSAL ANTI-CAVITY FLUORIDE
- Generic name
- SODIUM MONOFLUOROPHOSPHATE
- Manufacturer
- Universal Distribution Center LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e3356374-befa-41b0-ab0f-edfd5a062601
- SPL ID
- 42b18d2a-c986-42a0-9f88-9ee8e8b1290b
- Version
- 2
- Effective date
- 2023-11-16
- Source export date
- 2026-10-12
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:26:48
| 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 | UNIVERSAL ANTI-CAVITY FLUORIDE | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE | openfda.generic_name | |
| manufacturer name | Universal Distribution Center LLC | openfda.manufacturer_name | |
| ndc | package | 52000-111-01 | openfda.package_ndc |
| ndc | product | 52000-111 | openfda.product_ndc |
| ndc11 | package | 52000011101 | derived:openfda.package_ndc |
| rxcui | 545626 | openfda.rxcui | |
| spl id | 42b18d2a-c986-42a0-9f88-9ee8e8b1290b | id | |
| spl set id | e3356374-befa-41b0-ab0f-edfd5a062601 | 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.