warnings
WARNINGS WHEN USING THIS PRODUCT DO NOT SWALLOW UNLESS TOLD TO DO SO BY A DENTIST OR PHYSICIAN.
NEUTRA MAXX 5000
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
- NEUTRA MAXX 5000
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Massco Dental A Division of Dunagin Pharmaceuticals
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- fcbe6baa-2827-49df-9316-42cc86595203
- SPL ID
- cb8064d7-2d0f-4860-b794-d90a121761ad
- Version
- 7
- Effective date
- 2023-12-17
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:31:02
| Harmonized routes |
|---|
| ORAL |
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 | NEUTRA MAXX 5000 | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Massco Dental A Division of Dunagin Pharmaceuticals | openfda.manufacturer_name | |
| ndc | package | 63783-504-06 | openfda.package_ndc |
| ndc | product | 63783-504 | openfda.product_ndc |
| ndc11 | package | 63783050406 | derived:openfda.package_ndc |
| rxcui | 1191716 | openfda.rxcui | |
| rxcui | 392038 | openfda.rxcui | |
| spl id | cb8064d7-2d0f-4860-b794-d90a121761ad | id | |
| spl set id | fcbe6baa-2827-49df-9316-42cc86595203 | 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.