NDC 44038-0680 - Hello Magical Mermaid
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
- 44038-0680
- Package NDCs from labels
- 44038-0680-1
- Manufacturer
- Accupac LLC
- Effective date
- 2024-09-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hello Magical Mermaid - Accupac LLC | Accupac LLC | 2024-09-24 | 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 |
|---|---|---|---|---|---|---|
| KOLORZ NEUTRAL FLUORIDE FOAM TRIPLE MINT | SODIUM FLUORIDE | DMG AMERICA, LLC | b83c62be-8e9d-4fa2-aa10-d34c88bf2387 | 2021-10-01 | Warnings | 8ZYQ1474W7 |
| KOLORZ SIXTY SECOND FLUORIDE FOAM TRIPLE MINT | SODIUM FLUORIDE | DMG AMERICA, LLC | 427f25e6-e50a-407a-a6f0-512123e381e4 | 2021-10-01 | Warnings | 8ZYQ1474W7 |
| Sterile Water | STERILE WATER | B. Braun Medical Inc. | d99f9133-e4d0-4dee-b611-dbc3f918b547 | 2021-08-09 | Warnings, Adverse reactions | 059QF0KO0R |
| Sterile Water | WATER | B. Braun Medical Inc. | 8924e52e-8622-4ed6-a061-1908183e0a18 | 2021-08-06 | Warnings, Adverse reactions | 059QF0KO0R |
| Eyewash | EYEWASH | Global Equipment Company | c4f78121-4668-2e0c-e053-2995a90ab6c6 | 2021-06-17 | Warnings | 059QF0KO0R |
| 8.4% SODIUM BICARBONATE | 8.4% SODIUM BICARBONATE | HF Acquisition Co. LLC, DBA HealthFirst | 74d8bb7a-9e7a-105f-e053-2a91aa0aec92 | 2021-05-03 | Warnings, Adverse reactions | 8MDF5V39QO |
| SODIUM BICARBONATE | SODIUM BICARBONATE | Medical Purchasing Solutions, LLC | bfc9c321-665c-ca97-e053-2995a90a7954 | 2021-04-12 | Warnings, Adverse reactions | 8MDF5V39QO |
| Wentworth Alcohol Free | SODIUM FLUORIDE | Sheffield Pharmaceuticals LLC | 5ed816ef-20bc-49ac-9202-8fac1edac579 | 2021-03-23 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Sodium Fluoride 5000 ppm Dry Mouth | SODIUM FLUORIDE | Sheffield Pharmaceuticals LLC | cbc67f03-55c4-4781-ba37-87c737b60282 | 2021-03-02 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Ionite APF | SODIUM FLUORIDE | Dharma Research, Inc. | ab9b07ad-f6b2-4289-bec4-fec58270dc97 | 2021-02-20 | Warnings | 8ZYQ1474W7 |
| Avant | SODIUM FLUORIDE | Dharma Research, Inc. | 4749dce1-c0b9-4737-8a30-85cd58aba21b | 2021-01-25 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Avant | SODIUM FLUORIDE | Dharma Research, Inc. | 184bbe52-3909-45f6-b4d0-fe7849fabc1c | 2021-01-25 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Sterile Water | WATER | Asclemed USA, Inc. | 45c38269-883c-4198-a9d5-03810a4420ec | 2021-01-14 | Warnings, Adverse reactions | 059QF0KO0R |
| Sodium Fluoride 5000 ppm Enamel Protect | SODIUM FLUORIDE1.1%, POTASSIUM NITRATE 5% | Sheffield Pharmaceuticals LLC | 83dfdead-4f71-404e-90ae-dbd6849c7cf1 | 2021-01-04 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Ionite APF Neutral | SODIUM FLUORIDE | Dharma Research, inc. | ad7a660b-274c-417e-bdf3-1d5addf06ad1 | 2020-11-18 | Warnings | 8ZYQ1474W7 |
| Ionite APF | SODIUM FLUORIDE | Dharma Research, inc. | 8ff1b377-0535-4548-a109-f9f1a43b85b7 | 2020-11-16 | Warnings | 8ZYQ1474W7 |
| Ionite APF | SODIUM FLUORIDE | Dharma Research, inc. | e6c31330-43e0-4d32-af54-ff852af39cab | 2020-11-16 | Warnings | 8ZYQ1474W7 |
| Ionite APF | SODIUM FLUORIDE | Dharma Research, inc. | bc9664df-c4eb-4d29-b1c0-4d4dff6a75e4 | 2020-11-16 | Warnings | 8ZYQ1474W7 |
| Good Sense Omeprazole and Sodium Bicarbonate | OMEPRAZOLE, SODIUM BICARBONATE | L. Perrigo Company | bcf32242-de17-4da1-b707-4ce26262eb78 | 2020-11-16 | Warnings | 8MDF5V39QO |
| Ionite APF | SODIUM FLUORIDE | Dharma Research, inc. | b8b7f9b8-ff11-4a76-ab36-7822c15e1892 | 2020-11-16 | Warnings | 8ZYQ1474W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.