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 Whitening KnockOut Fluoride
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 Whitening KnockOut Fluoride
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Colgate-Palmolive Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 92079d13-3b66-42b7-9990-2727a489b6f6
- SPL ID
- 80878d16-ec55-43da-bd7a-37f3b2c7529e
- Version
- 10
- Effective date
- 2026-07-28
- Source export date
- 2026-10-12
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:45:11
| 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 Whitening KnockOut Fluoride | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Colgate-Palmolive Company | openfda.manufacturer_name | |
| ndc | package | 35000-972-63 | openfda.package_ndc |
| ndc | package | 35000-972-99 | openfda.package_ndc |
| ndc | package | 35000-972-58 | openfda.package_ndc |
| ndc | package | 35000-972-60 | openfda.package_ndc |
| ndc | product | 35000-972 | openfda.product_ndc |
| ndc11 | package | 35000097299 | derived:openfda.package_ndc |
| ndc11 | package | 35000097260 | derived:openfda.package_ndc |
| ndc11 | package | 35000097258 | derived:openfda.package_ndc |
| ndc11 | package | 35000097263 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | 80878d16-ec55-43da-bd7a-37f3b2c7529e | id | |
| spl set id | 92079d13-3b66-42b7-9990-2727a489b6f6 | 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.