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 dial (412) 390-3381 right away (Poison Control Center).
TOMS OF MAINE KIDS SILLY STRAWBERRY
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
- TOMS OF MAINE KIDS SILLY STRAWBERRY
- Generic name
- SODIUM MONOFLUOROPHOSPHATE
- Manufacturer
- Tom's of Maine, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e36ceb7a-9a29-41d8-8d08-a859e515f1f5
- SPL ID
- 92bd8099-9b09-44ee-9475-2f16e6fd0d45
- Version
- 18
- Effective date
- 2026-08-13
- 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 06:28:31
| 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 | TOMS OF MAINE KIDS SILLY STRAWBERRY | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE | openfda.generic_name | |
| manufacturer name | Tom's of Maine, Inc. | openfda.manufacturer_name | |
| ndc | package | 51009-910-42 | openfda.package_ndc |
| ndc | package | 51009-910-53 | openfda.package_ndc |
| ndc | package | 51009-910-51 | openfda.package_ndc |
| ndc | package | 51009-910-52 | openfda.package_ndc |
| ndc | package | 51009-910-10 | openfda.package_ndc |
| ndc | package | 51009-910-01 | openfda.package_ndc |
| ndc | product | 51009-910 | openfda.product_ndc |
| ndc11 | package | 51009091042 | derived:openfda.package_ndc |
| ndc11 | package | 51009091010 | derived:openfda.package_ndc |
| ndc11 | package | 51009091051 | derived:openfda.package_ndc |
| ndc11 | package | 51009091052 | derived:openfda.package_ndc |
| ndc11 | package | 51009091053 | derived:openfda.package_ndc |
| ndc11 | package | 51009091001 | derived:openfda.package_ndc |
| rxcui | 545626 | openfda.rxcui | |
| spl id | 92bd8099-9b09-44ee-9475-2f16e6fd0d45 | id | |
| spl set id | e36ceb7a-9a29-41d8-8d08-a859e515f1f5 | 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.