warnings
Warning
Gel 1100 Mint
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
- Gel 1100 Mint
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Dental Alliance Holdings LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f125fb04-5045-5367-e053-2a95a90aa73b
- SPL ID
- 8c79367f-d60d-484b-8e32-87de7cf75358
- Version
- 3
- Effective date
- 2025-12-29
- 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 05:14:55
| 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 | Gel 1100 Mint | openfda.brand_name | |
| brand name | Gel 1100 Grape | openfda.brand_name | |
| brand name | Gel 1100 Citrus | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Dental Alliance Holdings LLC | openfda.manufacturer_name | |
| ndc | package | 61578-214-01 | openfda.package_ndc |
| ndc | package | 61578-213-01 | openfda.package_ndc |
| ndc | package | 61578-217-01 | openfda.package_ndc |
| ndc | package | 61578-213-02 | openfda.package_ndc |
| ndc | product | 61578-217 | openfda.product_ndc |
| ndc | product | 61578-214 | openfda.product_ndc |
| ndc | product | 61578-213 | openfda.product_ndc |
| ndc11 | package | 61578021701 | derived:openfda.package_ndc |
| ndc11 | package | 61578021302 | derived:openfda.package_ndc |
| ndc11 | package | 61578021301 | derived:openfda.package_ndc |
| ndc11 | package | 61578021401 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | 8c79367f-d60d-484b-8e32-87de7cf75358 | id | |
| spl set id | f125fb04-5045-5367-e053-2a95a90aa73b | 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.