NDC 83367-101-01 - Hoo Gargle Jasmine Mint 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
- 83367-101
- Requested NDC
- 83367-101-01
- Package NDCs from labels
- 83367-101-01, 83367-101-02, 83367-101-03, 83367-101-04, 83367-101-05, 83367-101-06, 83367-101-07, 83367-101-08
- Manufacturer
- Nuriearth Global Co., Ltd | Miko Co., Ltd.
- Effective date
- 2023-04-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hoo Gargle Jasmine Mint Flavor - Nuriearth Global Co., Ltd | Miko Co., Ltd. | Nuriearth Global Co., Ltd | Miko Co., Ltd. | 2023-04-12 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83367-101-01 | Hoo Gargle Jasmine Mint Flavor | 15 mL in 1 PACKET | LIQUID | 15 | 1 | |
| 83367-101-02 | Hoo Gargle Jasmine Mint Flavor | 1 in 1 PACKAGE | LIQUID | 1 | 1 | |
| 83367-101-03 | Hoo Gargle Jasmine Mint Flavor | 30 mL in 1 PACKET | LIQUID | 30 | 1 | |
| 83367-101-04 | Hoo Gargle Jasmine Mint Flavor | 1 in 1 PACKAGE | LIQUID | 1 | 1 | |
| 83367-101-05 | Hoo Gargle Jasmine Mint Flavor | 50 mL in 1 PACKET | LIQUID | 50 | 1 | |
| 83367-101-06 | Hoo Gargle Jasmine Mint Flavor | 1 in 1 PACKAGE | LIQUID | 1 | 1 | |
| 83367-101-07 | Hoo Gargle Jasmine Mint Flavor | 100 mL in 1 PACKET | LIQUID | 100 | 1 | |
| 83367-101-08 | Hoo Gargle Jasmine Mint Flavor | 1 in 1 PACKAGE | LIQUID | 1 | 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.
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| RockSauce Warming Massage Roll-On | MENTHOL, METHYL SALICYLATE | Implus Footcare, LLC | 5a2d9c3a-67fc-4c1a-b1e8-62a93880397a | 2026-01-29 | Warnings | L7T10EIP3A |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.