NDC 81840-3333-2 - Hoo gargle (apple spearmint flavor)
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
- 81840-3333
- Requested NDC
- 81840-3333-2
- Package NDCs from labels
- 81840-3333-0, 81840-3333-1, 81840-3333-2, 81840-3333-3, 81840-3333-4, 81840-3333-5
- Manufacturer
- MIKO CO LTD
- Effective date
- 2023-10-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hoo gargle (apple spearmint flavor) - MIKO CO LTD | MIKO CO LTD | 2023-10-06 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81840-3333-5 | 2024-07-30 | C162847 | 48780-1 | 1030e365-508e-111a-e063-dadaa90a10e2 | Drug Facts |
| 81840-3333-5 | 2024-01-30 | C162847 | 48780-1 | 1030e365-508e-111a-e063-dadaa90a10e2 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81840-3333-0 | Hoo gargle (apple spearmint flavor) | 10 mL in 1 POUCH | LIQUID | 10 | 4 | |
| 81840-3333-1 | Hoo gargle (apple spearmint flavor) | 10 in 1 PACKAGE | LIQUID | 10 | 4 | |
| 81840-3333-2 | Hoo gargle (apple spearmint flavor) | 15 in 1 PACKAGE | LIQUID | 15 | 4 | |
| 81840-3333-3 | Hoo gargle (apple spearmint flavor) | 30 in 1 PACKAGE | LIQUID | 30 | 4 | |
| 81840-3333-4 | Hoo gargle (apple spearmint flavor) | 50 in 1 PACKAGE | LIQUID | 50 | 4 | |
| 81840-3333-5 | Hoo gargle (apple spearmint flavor) | 100 in 1 PACKAGE | LIQUID | 100 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 81840-3333 | HOO GARGLE (APPLE SPEARMINT FLAVOR) (SODIUM FLOURIDE) LIQUID [MIKO CO LTD] | 4 | Legacy NDC, 6 package rows | 20231007_e9148945-57e6-2bba-e053-2995a90a8af3.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 |
|---|---|---|---|---|---|---|
| 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 |
| Ionite APF | SODIUM FLUORIDE | Dharma Research, inc. | b8b7f9b8-ff11-4a76-ab36-7822c15e1892 | 2020-11-16 | Warnings | 8ZYQ1474W7 |
| Ionite APF | SODIUM FLUORIDE | Dharma Research, inc. | e1797adf-4665-4322-a3aa-dd2da9dcd3a8 | 2020-11-16 | Warnings | 8ZYQ1474W7 |
| Ionite APF | SODIUM FLUORIDE | Dharma Research, inc. | ce34c159-34cd-47c7-937f-743b3309742b | 2020-11-16 | Warnings | 8ZYQ1474W7 |
| 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 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.