warnings
Warnings Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or dial (412) 390-3381 right away (Poison Control Center).
TOMS OF MAINE ACTIVATED CHARCOAL PEPPERMINT
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
- TOMS OF MAINE ACTIVATED CHARCOAL PEPPERMINT
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Tom's of Maine, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b9e6e455-8444-4805-89f1-ee9142f98e36
- SPL ID
- a8944014-cc00-41f7-8ac9-ccae8024644e
- Version
- 14
- Effective date
- 2026-08-10
- Source export date
- 2026-10-27
- 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/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:45:46
| 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 | TOMS OF MAINE ACTIVATED CHARCOAL PEPPERMINT | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Tom's of Maine, Inc. | openfda.manufacturer_name | |
| ndc | package | 51009-900-47 | openfda.package_ndc |
| ndc | package | 51009-900-40 | openfda.package_ndc |
| ndc | product | 51009-900 | openfda.product_ndc |
| ndc11 | package | 51009090040 | derived:openfda.package_ndc |
| ndc11 | package | 51009090047 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | a8944014-cc00-41f7-8ac9-ccae8024644e | id | |
| spl set id | b9e6e455-8444-4805-89f1-ee9142f98e36 | 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.