NDC 69255-500-01 - Doctor 9020 Dental Clinic
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
- 69255-500
- Requested NDC
- 69255-500-01
- Package NDCs from labels
- 69255-500-01, 69255-500-02
- Manufacturer
- JANGIN PHARM CO.,LTD.
- Effective date
- 2019-12-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Doctor 9020 Dental Clinic - JANGIN PHARM CO.,LTD. | JANGIN PHARM CO.,LTD. | 2019-12-15 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69255-500-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-20a5-a910-e053-dadaa90a0b85 | 99ca7d9b-44c0-b1ac-e053-2995a90aecd8 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69255-500-01 | Doctor 9020 Dental Clinic | 12 mL in 1 POUCH | LIQUID | 12 | 1 | |
| 69255-500-02 | Doctor 9020 Dental Clinic | 15 in 1 PACKAGE | LIQUID | 15 | 1 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Ionite APF | SODIUM FLUORIDE | Dharma Research, inc. | 503ca71a-f50c-4406-b925-5b6ac36a9212 | 2020-11-15 | Warnings | 8ZYQ1474W7 |
| Ionite R | SODIUM FLUORIDE | Dharma Research, Inc. | 1009afc7-6e9d-417f-a702-f8a941e08484 | 2020-11-06 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Ionite R | SODIUM FLUORIDE | Dharma Research, Inc. | 0e7b3eb3-3a9e-4a51-b2b5-9f36876fc8a5 | 2020-11-06 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Ionite APF Foam | SODIUM FLUORIDE | Dharma Research, inc. | d22afac7-45d6-467e-951a-e7c241b9180d | 2020-10-27 | Warnings | 8ZYQ1474W7 |
| Ionite APF Foam | SODIUM FLUORIDE | Dharma Research, inc. | 4828b482-486f-4105-bed0-3fe2ddbbddb1 | 2020-10-27 | Warnings | 8ZYQ1474W7 |
| Ionite APF Foam | SODIUM FLUORIDE | Dharma Research, Inc. | 8987b447-3fa3-4f52-aecc-80e44c981aaa | 2020-10-27 | Warnings | 8ZYQ1474W7 |
| Ionite APF Neutral | SODIUM FLUORIDE | Dharma Research, inc. | 8191554f-adb6-4ba9-aa80-0a9bb65193ec | 2020-10-27 | Warnings | 8ZYQ1474W7 |
| Ionite APF Foam | SODIUM FLUORIDE | Dharma Research, inc. | ddd34623-cb79-4fa7-bd01-19122470b63d | 2020-10-27 | Warnings | 8ZYQ1474W7 |
| FluoriMax 5000 | 1.1% SODIUM FLUORIDE TOOTHPASTE | Elevate Oral Care | ae45ae2d-a21f-0a05-e053-2995a90a4d5e | 2020-09-01 | Warnings | 8ZYQ1474W7 |
| FluoriMax 5000 Sensitive | 1.1% SODIUM FLUORIDE WITH 5% POTASSIUM NITRATE TOOTHPASTE | Elevate Oral Care | ae32b0a2-e42f-6a56-e053-2a95a90a0b00 | 2020-08-31 | Warnings | 8ZYQ1474W7 |
| Sodium Fluoride 5000 ppm Sensitive | SODIUM FLUORIDE1.1%, POTASSIUM NITRATE 5% | Sheffield Pharmaceuticals LLC | 02f4cf0b-188c-4522-b759-ffe4a9d150e8 | 2020-04-01 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| 99ca624d-733d-59fa-e053-2a95a90a5c92 | 99ca7d9b-44c0-b1ac-e053-2995a90aecd8 | 2019-12-15 | Warnings | 99ca624d-733d-59fa-e053-2a95a90a5c92 99ca7d9b-44c0-b1ac-e053-2995a90aecd8 | ||
| 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 |
| 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 |
| Pain Relief | DL-CAMPHOR, L-MENTHOL, METHYL SALICYLATE PATCH | Kareway Product, Inc. | d3ede306-9ef7-4a89-896b-c083f6e43c85 | 2017-12-05 | Warnings | BZ1R15MTK7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.