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 OPTIC WHITE PRO SERIES ENAMEL RENEWAL SOOTHING 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 OPTIC WHITE PRO SERIES ENAMEL RENEWAL SOOTHING MINT
- Generic name
- SODIUM MONOFLUOROPHOSPHATE
- Manufacturer
- Colgate-Palmolive Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cd954777-697a-4cc7-8f5f-b2caf357ef95
- SPL ID
- 922a6319-363a-48f5-81dc-934fa738bb9d
- Version
- 3
- Effective date
- 2026-08-13
- 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 02:29:32
| 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 OPTIC WHITE PRO SERIES ENAMEL RENEWAL SOOTHING MINT | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE | openfda.generic_name | |
| manufacturer name | Colgate-Palmolive Company | openfda.manufacturer_name | |
| ndc | package | 35000-791-62 | openfda.package_ndc |
| ndc | package | 35000-791-63 | openfda.package_ndc |
| ndc | product | 35000-791 | openfda.product_ndc |
| ndc11 | package | 35000079163 | derived:openfda.package_ndc |
| ndc11 | package | 35000079162 | derived:openfda.package_ndc |
| rxcui | 1038995 | openfda.rxcui | |
| spl id | 922a6319-363a-48f5-81dc-934fa738bb9d | id | |
| spl set id | cd954777-697a-4cc7-8f5f-b2caf357ef95 | 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.