NDC 50555-220-01 - Foamgle Foam Super Mint
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
- 50555-220
- Requested NDC
- 50555-220-01
- Package NDCs from labels
- 50555-220-01, 50555-220-02
- Manufacturer
- KMPHARMACEUTICAL CO.,LTD | KMPHARMACEUTICAL Co.,Ltd.
- Effective date
- 2026-03-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Foamgle Foam Mouthwash – Super Mint 150mL | KMPHARMACEUTICAL CO.,LTD | KMPHARMACEUTICAL Co.,Ltd. | 2026-03-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50555-220-01 | Foamgle Foam Super Mint | 150 mL in 1 BOTTLE | MOUTHWASH | 150 | 1 | |
| 50555-220-02 | Foamgle Foam Super Mint | 1 in 1 CARTON | MOUTHWASH | 1 | 1 |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.