warnings
Warnings Stop use and ask a dentist if oral irritation or tooth sensitivity occurs 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 Whitening Anticavity Gentle 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
- ACT Whitening Anticavity Gentle Mint
- Generic name
- SODIUM FLUORIDE 0.02 (0.009 W/V FLUORIDE ION)
- Manufacturer
- Chattem, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cd45a0b8-9ab3-4aed-8214-a6dcc4cdaf49
- SPL ID
- e0e0a4a0-368c-4b6c-94bb-0988f3d8cc58
- Version
- 5
- Effective date
- 2026-01-12
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:02:55
| 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 |
|---|---|---|---|
| application number | M021 | openfda.application_number | |
| brand name | ACT Whitening Anticavity Gentle Mint | openfda.brand_name | |
| generic name | SODIUM FLUORIDE 0.02 (0.009 W/V FLUORIDE ION) | openfda.generic_name | |
| manufacturer name | Chattem, Inc. | openfda.manufacturer_name | |
| ndc | package | 41167-0983-2 | openfda.package_ndc |
| ndc | product | 41167-0983 | openfda.product_ndc |
| ndc11 | package | 41167098302 | derived:openfda.package_ndc |
| rxcui | 1044540 | openfda.rxcui | |
| rxcui | 313029 | openfda.rxcui | |
| spl id | e0e0a4a0-368c-4b6c-94bb-0988f3d8cc58 | id | |
| spl set id | cd45a0b8-9ab3-4aed-8214-a6dcc4cdaf49 | 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.