NDC 76357-290 - SmartMouth Clinical Gum and Plaque Formula
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
- 76357-290
- Package NDCs from labels
- 76357-290-01
- Manufacturer
- Triumph Pharmaceuticals Inc.
- Effective date
- 2024-12-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SmartMouth Gum and Plaque Solution 1 - Triumph Pharmaceuticals Inc. | Triumph Pharmaceuticals Inc. | 2024-12-11 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76357-290-01 | SmartMouth Clinical Gum and Plaque Formula | 296 mL in 1 BOTTLE, PLASTIC | LIQUID | 296 mL | 500 mg in 20mL | 8 |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.