NDC 0273-8010-01 - NAFRINSE PACKETSKIT VERY BERRY
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
- 0273-8010
- Requested NDC
- 0273-8010-01
- Package NDCs from labels
- 0273-8010-01, 0273-8010-02
- Manufacturer
- Young Dental Manufacturing Co 1, LLC. | Medical Products Laboratories, Inc
- Effective date
- 2018-12-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| NAFRINSE PACKETSKIT VERY BERRY - Young Dental Manufacturing Co 1, LLC. | Medical Products Laboratories, Inc | Young Dental Manufacturing Co 1, LLC. | Medical Products Laboratories, Inc | 2018-12-14 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0273-8010-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-c3d0-f424-e053-dadaa90a57ce | Convinience KIT -20 pack of Nafrinse packets, a polyethylene jug, dispenser pump, plastic cups, paper napkins, and trash bag with ties |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0273-8010-01 | NAFRINSE PACKETSKIT VERY BERRY | 3 g in 1 PACKET | POWDER | 3 | 2 | |
| 0273-8010-02 | NAFRINSE PACKETSKIT VERY BERRY | 20 in 1 KIT | POWDER | 20 | 2 |
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 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 |
| CPDA-1 | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE | Fenwal, Inc. | ee831456-5962-4d5e-ad0c-69ab85860453 | 2020-06-03 | XF417D3PSL | |
| 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 |
| Renacidin | CITRIC ACID, GLUCONOLACTONE AND MAGNESIUM CARBONATE | United-Guardian, Inc. | 13a9bbba-db21-4cba-991c-5d8afaf2ed74 | 2019-12-17 | Warnings, Adverse reactions | XF417D3PSL |
| PreviDent 5000 Sensitive | SODIUM FLUORIDE AND POTASSIUM NITRATE | Colgate Oral Pharmaceuticals, Inc. | b028cfff-4946-49e8-b8bb-197ab99d0d35 | 2019-12-09 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| CPDA-1 | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE | Fenwal, Inc. | e41adb4e-06fb-4141-ba55-50b043f3c9da | 2019-11-19 | XF417D3PSL | |
| CPDA-1 | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE | Fenwal, Inc. | 14445dfd-6041-40cd-a043-3f4da6bcb9c1 | 2019-11-18 | XF417D3PSL | |
| CPDA-1 | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE | Fenwal, Inc. | 2557199a-5f60-49d8-b093-1e0700211243 | 2019-11-18 | XF417D3PSL | |
| CPDA-1 | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE | Fenwal, Inc. | 794f724c-87f0-49c1-9b26-c9e491978313 | 2019-11-18 | XF417D3PSL | |
| CPDA-1 | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE | Fenwal, Inc. | 5c7d3287-883a-459b-9214-074a583c8a59 | 2019-11-18 | XF417D3PSL | |
| CPDA-1 | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE | Fenwal, Inc. | 448a1dc5-7a98-4b2f-82af-4b92de05cfc3 | 2019-11-18 | XF417D3PSL | |
| 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 | 562510 8ZYQ1474W7 |
| FLUORIDEX | SODIUM FLUORIDE | DEN-MAT HOLDINGS, LLC. | 6014c330-3698-027c-e053-2a91aa0a64e5 | 2019-02-28 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| 311c6396-5463-4fc8-99fb-d4d6a3db4eaa | 97f64104-21b1-4fb3-a9d4-f1c17b8ae2b4 | 2018-12-14 | Warnings | 311c6396-5463-4fc8-99fb-d4d6a3db4eaa 97f64104-21b1-4fb3-a9d4-f1c17b8ae2b4 | ||
| 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 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.