NDC 52257-1380-02 - 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
- 52257-1380-02
- Package NDCs from labels
- 52257-1380-1, 52257-1380-2, 52257-1380-02
- 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SF 5000 Plus | 1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM | Cypress Pharmaceutical, Inc. | fa625ece-d873-491a-8d45-2833b64e5425 | 2016-07-01 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 54c1a27c-5936-4ee2-a419-3891d3df9745 | 2015-08-02 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 642fec99-c5c5-4ef2-986e-5b5f7cf460de | 2015-08-02 | Warnings, Adverse reactions | 8ZYQ1474W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.