warnings
Warnings: Ask a doctor before use if you have: Bleeding or redness lasting more than 2 weeks. Pain, swelling, pus, loose teeth, or more spacing between teeth. These may be signs of periodontitis, a serious form of gum disease.
ATOMY PROPOLIS TOOTHPAS TE 50G
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
- ATOMY PROPOLIS TOOTHPAS TE 50G
- Generic name
- SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE
- Manufacturer
- ATOMY CO., LTD.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 98d839e3-a1aa-c83d-e053-2995a90a7e79
- SPL ID
- bf9632ba-2fdb-4d32-b069-b2533e94f974
- Version
- 5
- Effective date
- 2024-01-30
- Source export date
- 2026-09-28
- 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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:18:14
| 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 | ATOMY PROPOLIS TOOTHPAS TE 50G | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | ATOMY CO., LTD. | openfda.manufacturer_name | |
| ndc | package | 52257-1380-2 | openfda.package_ndc |
| ndc | package | 52257-1380-1 | openfda.package_ndc |
| ndc | product | 52257-1380 | openfda.product_ndc |
| ndc11 | package | 52257138002 | derived:openfda.package_ndc |
| ndc11 | package | 52257138001 | derived:openfda.package_ndc |
| rxcui | 1046867 | openfda.rxcui | |
| spl id | bf9632ba-2fdb-4d32-b069-b2533e94f974 | id | |
| spl set id | 98d839e3-a1aa-c83d-e053-2995a90a7e79 | set_id | |
| unii | 8ZYQ1474W7 | openfda.unii | |
| 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.