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 BAKING SODA AND PEROXIDE WHITENING OXYGEN BUBBLES FROSTY 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 BAKING SODA AND PEROXIDE WHITENING OXYGEN BUBBLES FROSTY MINT
- Generic name
- SODIUM MONOFLUOROPHOSPHATE
- Manufacturer
- Colgate-Palmolive Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 263fef13-347b-489b-987d-933a63dbc900
- SPL ID
- 59ae8eda-bcf0-4f0a-baa0-7049a09a0914
- Version
- 12
- Effective date
- 2026-07-08
- Source export date
- 2026-11-06
- 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/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:53:51
| 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 BAKING SODA AND PEROXIDE WHITENING OXYGEN BUBBLES FROSTY MINT | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE | openfda.generic_name | |
| manufacturer name | Colgate-Palmolive Company | openfda.manufacturer_name | |
| ndc | package | 35000-960-69 | openfda.package_ndc |
| ndc | package | 35000-960-82 | openfda.package_ndc |
| ndc | package | 35000-960-60 | openfda.package_ndc |
| ndc | package | 35000-960-64 | openfda.package_ndc |
| ndc | package | 35000-960-35 | openfda.package_ndc |
| ndc | product | 35000-960 | openfda.product_ndc |
| ndc11 | package | 35000096069 | derived:openfda.package_ndc |
| ndc11 | package | 35000096082 | derived:openfda.package_ndc |
| ndc11 | package | 35000096035 | derived:openfda.package_ndc |
| ndc11 | package | 35000096064 | derived:openfda.package_ndc |
| ndc11 | package | 35000096060 | derived:openfda.package_ndc |
| rxcui | 545626 | openfda.rxcui | |
| spl id | 59ae8eda-bcf0-4f0a-baa0-7049a09a0914 | id | |
| spl set id | 263fef13-347b-489b-987d-933a63dbc900 | set_id | |
| unii | C810JCZ56Q | 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.