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 Kids Cavity Protection
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 Kids Cavity Protection
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Colgate-Palmolive Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f0e68196-8566-443b-9cc8-b57d5c001558
- SPL ID
- d203ad42-ee3f-42fa-9213-6cf6026117ca
- Version
- 4
- Effective date
- 2026-10-19
- Source export date
- 2026-10-23
- 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/2026-10-23/e2a780351c9d52ec13a8c93757e95e68824c68ebed04761d4eea108c6b76cf54/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 003b0607e7bf4d3ce17ccc0942e221303b4f62b17a6a00c54547eda454293380
- Import run
- 20261026T035824Z
- Imported at
- 2026-10-26 04:30:37
| 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 Kids Cavity Protection | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Colgate-Palmolive Company | openfda.manufacturer_name | |
| ndc | package | 35000-015-59 | openfda.package_ndc |
| ndc | package | 35000-015-32 | openfda.package_ndc |
| ndc | package | 35000-015-47 | openfda.package_ndc |
| ndc | package | 35000-015-24 | openfda.package_ndc |
| ndc | package | 35000-015-46 | openfda.package_ndc |
| ndc | package | 35000-015-20 | openfda.package_ndc |
| ndc | package | 35000-015-45 | openfda.package_ndc |
| ndc | product | 35000-015 | openfda.product_ndc |
| ndc11 | package | 35000001545 | derived:openfda.package_ndc |
| ndc11 | package | 35000001532 | derived:openfda.package_ndc |
| ndc11 | package | 35000001559 | derived:openfda.package_ndc |
| ndc11 | package | 35000001524 | derived:openfda.package_ndc |
| ndc11 | package | 35000001520 | derived:openfda.package_ndc |
| ndc11 | package | 35000001547 | derived:openfda.package_ndc |
| ndc11 | package | 35000001546 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | d203ad42-ee3f-42fa-9213-6cf6026117ca | id | |
| spl set id | f0e68196-8566-443b-9cc8-b57d5c001558 | 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.