warnings
W arnings 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.
ACT Restoring Anticavity Fluoride Mint Burst
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
- ACT Restoring Anticavity Fluoride Mint Burst
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Chattem, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a38363e6-7105-4663-95a0-09ecb2948f83
- SPL ID
- c8d906b9-c4c5-425f-8955-e3b451311e74
- Version
- 8
- Effective date
- 2025-09-30
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:26:06
| 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 | ACT Restoring Anticavity Fluoride Mint Burst | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Chattem, Inc. | openfda.manufacturer_name | |
| ndc | package | 41167-0979-1 | openfda.package_ndc |
| ndc | package | 41167-0979-0 | openfda.package_ndc |
| ndc | package | 41167-0979-3 | openfda.package_ndc |
| ndc | product | 41167-0979 | openfda.product_ndc |
| ndc11 | package | 41167097900 | derived:openfda.package_ndc |
| ndc11 | package | 41167097901 | derived:openfda.package_ndc |
| ndc11 | package | 41167097903 | derived:openfda.package_ndc |
| rxcui | 240698 | openfda.rxcui | |
| rxcui | 656809 | openfda.rxcui | |
| spl id | c8d906b9-c4c5-425f-8955-e3b451311e74 | id | |
| spl set id | a38363e6-7105-4663-95a0-09ecb2948f83 | 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.