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 MaxFresh with Mini Breath Clean 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
- Colgate MaxFresh with Mini Breath Clean Mint
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Colgate-Palmolive Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 82bc1101-84d7-4e21-be9c-870ad88a4b7c
- SPL ID
- e6c8cb12-5fdc-4a5d-855e-e68e1f156b17
- Version
- 18
- Effective date
- 2024-11-14
- 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 06:27:04
| 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 MaxFresh with Mini Breath Clean Mint | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Colgate-Palmolive Company | openfda.manufacturer_name | |
| ndc | package | 35000-013-60 | openfda.package_ndc |
| ndc | package | 35000-013-78 | openfda.package_ndc |
| ndc | package | 35000-013-97 | openfda.package_ndc |
| ndc | package | 35000-013-95 | openfda.package_ndc |
| ndc | package | 35000-013-30 | openfda.package_ndc |
| ndc | package | 35000-013-74 | openfda.package_ndc |
| ndc | package | 35000-013-34 | openfda.package_ndc |
| ndc | product | 35000-013 | openfda.product_ndc |
| ndc11 | package | 35000001360 | derived:openfda.package_ndc |
| ndc11 | package | 35000001378 | derived:openfda.package_ndc |
| ndc11 | package | 35000001334 | derived:openfda.package_ndc |
| ndc11 | package | 35000001330 | derived:openfda.package_ndc |
| ndc11 | package | 35000001395 | derived:openfda.package_ndc |
| ndc11 | package | 35000001397 | derived:openfda.package_ndc |
| ndc11 | package | 35000001374 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | e6c8cb12-5fdc-4a5d-855e-e68e1f156b17 | id | |
| spl set id | 82bc1101-84d7-4e21-be9c-870ad88a4b7c | 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.