NDC 52257-1360-1 - ATOMY PROPOLIS TOOTHPAS TE 200g
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
- 52257-1360
- Requested NDC
- 52257-1360-1
- Package NDCs from labels
- 52257-1360-1, 52257-1360-2
- Manufacturer
- ATOMY CO., LTD. | Kolmar Korea Co., Ltd.
- Effective date
- 2016-10-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ATOMY PROPOLIS TOOTHPAS TE 200g - ATOMY CO., LTD. | Kolmar Korea Co., Ltd. | ATOMY CO., LTD. | Kolmar Korea Co., Ltd. | 2016-10-10 | HUMAN OTC DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| 82d723b3-203b-477c-bc61-5efd70e673d4 | 2989ae59-ac06-4374-8516-53bf14f4fd73 | 2019-12-23 | Warnings | 2989ae59-ac06-4374-8516-53bf14f4fd73 | ||
| PreviDent 5000 Sensitive | SODIUM FLUORIDE AND POTASSIUM NITRATE | Colgate Oral Pharmaceuticals, Inc. | b028cfff-4946-49e8-b8bb-197ab99d0d35 | 2019-12-09 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| KOLORZ SIXTY SECOND FLUORIDE TRIPLE MINT | SODIUM FLUORIDE | DMG AMERICA, LLC | 21fa26f2-0162-4044-aec0-d5360be3f3e0 | 2019-03-28 | Warnings | 8ZYQ1474W7 |
| FLUORIDEX | SODIUM FLUORIDE | DEN-MAT HOLDINGS, LLC. | 5fd60635-4b66-15e3-e053-2991aa0ab23a | 2019-02-28 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Pro-Den Rx | SODIUM FLUORIDE | Den-mat Holdings, Llc | e39b19f7-2b3e-4c77-9544-623ebad84870 | 2019-02-28 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| FLUORIDEX | SODIUM FLUORIDE | DEN-MAT HOLDINGS, LLC. | 6014c330-3698-027c-e053-2a91aa0a64e5 | 2019-02-28 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Plus White | SODIUM MONOFLUOROPHOSPHATE | CCA Industries, Inc. | 7581b27b-6acb-45b0-8804-b5dae3498931 | 2018-08-01 | Warnings | C810JCZ56Q |
| Pro-Den Rx | SODIUM FLUORIDE | Den-Mat Holdings, Llc | ba020e07-ad41-4419-a503-f1245131b7d2 | 2018-04-17 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Sensitive Tooth Polish | POTASSIUM NITRATE AND SODIUM FLUORIDE | Melaleuca, Inc. | 689349e4-3980-a0e4-e053-2991aa0a9ef5 | 2018-03-29 | Warnings | 8ZYQ1474W7 |
| Homeoplex D | GLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM, | Supplement Clinic, LLC. | cd6b48ab-3566-484d-8deb-15ef6f8e7e8f | 2017-11-01 | Warnings | 506T60A25R |
| SF | 1.1% SODIUM FLUORIDE | Cypress Pharmaceutical, Inc. | b7c0a768-7e8a-40b9-876f-b86d3dc5e848 | 2016-07-06 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| 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 |
| 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.