warnings
Warnings • Do not swallow Keep out of reach of children under 6 years of age If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.
Morning Fresh
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
- Morning Fresh
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Dynarex Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1d0457d7-0228-4ea3-9755-73bacd2201e6
- SPL ID
- 2a44c697-3bbf-1352-e063-6394a90afa61
- Version
- 7
- Effective date
- 2024-12-27
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:58
| Harmonized routes |
|---|
| ORAL |
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 | Morning Fresh | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Dynarex Corporation | openfda.manufacturer_name | |
| ndc | package | 67777-175-12 | openfda.package_ndc |
| ndc | package | 67777-175-01 | openfda.package_ndc |
| ndc | package | 67777-175-11 | openfda.package_ndc |
| ndc | package | 67777-175-13 | openfda.package_ndc |
| ndc | package | 67777-175-10 | openfda.package_ndc |
| ndc | package | 67777-175-02 | openfda.package_ndc |
| ndc | product | 67777-175 | openfda.product_ndc |
| ndc11 | package | 67777017501 | derived:openfda.package_ndc |
| ndc11 | package | 67777017502 | derived:openfda.package_ndc |
| ndc11 | package | 67777017510 | derived:openfda.package_ndc |
| ndc11 | package | 67777017513 | derived:openfda.package_ndc |
| ndc11 | package | 67777017511 | derived:openfda.package_ndc |
| ndc11 | package | 67777017512 | derived:openfda.package_ndc |
| rxcui | 545626 | openfda.rxcui | |
| spl id | 2a44c697-3bbf-1352-e063-6394a90afa61 | id | |
| spl set id | 1d0457d7-0228-4ea3-9755-73bacd2201e6 | 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.