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 contact a Poison Control Center right away.
Colgate Triple Action
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
- Colgate Triple Action
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Colgate-Palmolive Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3082e9ba-66d9-4fc7-bbe6-b41b60939bd2
- SPL ID
- 905181e2-96e2-4b14-9605-47353a251173
- Version
- 16
- Effective date
- 2026-07-08
- Source export date
- 2026-10-12
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:28:56
| 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 | Colgate Triple Action | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Colgate-Palmolive Company | openfda.manufacturer_name | |
| ndc | package | 35000-941-69 | openfda.package_ndc |
| ndc | package | 35000-941-46 | openfda.package_ndc |
| ndc | package | 35000-941-58 | openfda.package_ndc |
| ndc | package | 35000-941-64 | openfda.package_ndc |
| ndc | package | 35000-941-99 | openfda.package_ndc |
| ndc | package | 35000-941-48 | openfda.package_ndc |
| ndc | package | 35000-941-92 | openfda.package_ndc |
| ndc | package | 35000-941-63 | openfda.package_ndc |
| ndc | package | 35000-941-82 | openfda.package_ndc |
| ndc | package | 35000-941-30 | openfda.package_ndc |
| ndc | package | 35000-941-47 | openfda.package_ndc |
| ndc | package | 35000-941-79 | openfda.package_ndc |
| ndc | package | 35000-941-60 | openfda.package_ndc |
| ndc | product | 35000-941 | openfda.product_ndc |
| ndc11 | package | 35000094163 | derived:openfda.package_ndc |
| ndc11 | package | 35000094147 | derived:openfda.package_ndc |
| ndc11 | package | 35000094199 | derived:openfda.package_ndc |
| ndc11 | package | 35000094146 | derived:openfda.package_ndc |
| ndc11 | package | 35000094164 | derived:openfda.package_ndc |
| ndc11 | package | 35000094192 | derived:openfda.package_ndc |
| ndc11 | package | 35000094130 | derived:openfda.package_ndc |
| ndc11 | package | 35000094148 | derived:openfda.package_ndc |
| ndc11 | package | 35000094182 | derived:openfda.package_ndc |
| ndc11 | package | 35000094158 | derived:openfda.package_ndc |
| ndc11 | package | 35000094160 | derived:openfda.package_ndc |
| ndc11 | package | 35000094169 | derived:openfda.package_ndc |
| ndc11 | package | 35000094179 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | 905181e2-96e2-4b14-9605-47353a251173 | id | |
| spl set id | 3082e9ba-66d9-4fc7-bbe6-b41b60939bd2 | 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.