NDC 52257-1380-01 - ATOMY PROPOLIS TOOTHPAS TE 50G
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 52257-1380
- Requested NDC
- 52257-1380-01
- Package NDCs from labels
- 52257-1380-1, 52257-1380-2, 52257-1380-01
- Manufacturer
- ATOMY CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong 2 factory
- Effective date
- 2024-01-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FLUORIDE ION - ATOMY CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong 2 factory | ATOMY CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong 2 factory | 2024-01-30 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52257-1380-1 | ATOMY PROPOLIS TOOTHPAS TE 50G | 50 g in 1 TUBE | PASTE, DENTIFRICE | 50 | 5 | |
| 52257-1380-2 | ATOMY PROPOLIS TOOTHPAS TE 50G | 4 in 1 CARTON | PASTE, DENTIFRICE | 4 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52257-1380 | ATOMY PROPOLIS TOOTHPAS TE 50G (SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [ATOMY CO., LTD.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20240130_98d839e3-a1aa-c83d-e053-2995a90a7e79.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.