warnings
Warnings Warnings Keep out of reach of children If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).
GuruNanda Anti-Cavity
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
- GuruNanda Anti-Cavity
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- GURUNANDA, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3b07b72f-4efc-eb0f-e063-6294a90a70a8
- SPL ID
- 48c6afc2-5f69-09e2-e063-6294a90ada5d
- Version
- 6
- Effective date
- 2026-01-19
- Source export date
- 2026-11-06
- 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/2026-11-06/2cac198adf50bf0f7077ca012f418bbee1fb171f907f83d6a83048d9770d345b/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 08:11:03
| 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 |
|---|---|---|---|
| application number | M021 | openfda.application_number | |
| brand name | GuruNanda Anti-Cavity | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | GURUNANDA, LLC | openfda.manufacturer_name | |
| ndc | package | 70708-890-16 | openfda.package_ndc |
| ndc | package | 70708-890-33 | openfda.package_ndc |
| ndc | package | 70708-890-24 | openfda.package_ndc |
| ndc | product | 70708-890 | openfda.product_ndc |
| ndc11 | package | 70708089033 | derived:openfda.package_ndc |
| ndc11 | package | 70708089016 | derived:openfda.package_ndc |
| ndc11 | package | 70708089024 | derived:openfda.package_ndc |
| rxcui | 240698 | openfda.rxcui | |
| spl id | 48c6afc2-5f69-09e2-e063-6294a90ada5d | id | |
| spl set id | 3b07b72f-4efc-eb0f-e063-6294a90a70a8 | 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.