warnings
Warnings Warnings
FluoriMax 5000 Sensitive
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
- FluoriMax 5000 Sensitive
- Generic name
- 1.1% SODIUM FLUORIDE WITH 5% POTASSIUM NITRATE TOOTHPASTE
- Manufacturer
- Elevate Oral Care
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d9f232c0-d154-536b-e053-2995a90af37d
- SPL ID
- 3f2bd1e3-4ba2-1bdb-e063-6294a90af9b0
- Version
- 2
- Effective date
- 2025-09-19
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:40:43
| Harmonized routes |
|---|
| TOPICAL |
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 |
|---|---|---|---|
| brand name | FluoriMax 5000 Sensitive | openfda.brand_name | |
| generic name | 1.1% SODIUM FLUORIDE WITH 5% POTASSIUM NITRATE TOOTHPASTE | openfda.generic_name | |
| manufacturer name | Elevate Oral Care | openfda.manufacturer_name | |
| ndc | package | 57511-0503-2 | openfda.package_ndc |
| ndc | package | 57511-0503-1 | openfda.package_ndc |
| ndc | product | 57511-0503 | openfda.product_ndc |
| ndc11 | package | 57511050302 | derived:openfda.package_ndc |
| ndc11 | package | 57511050301 | derived:openfda.package_ndc |
| rxcui | 637365 | openfda.rxcui | |
| rxcui | 2603764 | openfda.rxcui | |
| spl id | 3f2bd1e3-4ba2-1bdb-e063-6294a90af9b0 | id | |
| spl set id | d9f232c0-d154-536b-e053-2995a90af37d | set_id | |
| unii | 8ZYQ1474W7 | openfda.unii | |
| unii | RU45X2JN0Z | 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.