NDC 87548-010-01 - Osstem S Sensitivity relief tooth
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
- 87548-010
- Requested NDC
- 87548-010-01
- Package NDCs from labels
- 87548-010-01, 87548-010-02
- Manufacturer
- Osstem Pharma Co., Ltd | DONG IL PHARMS CO., LTD.
- Effective date
- 2026-04-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Osstem S Sensitivity Relief Toothpaste | Osstem Pharma Co., Ltd | DONG IL PHARMS CO., LTD. | 2026-04-15 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87548-010-01 | Osstem S Sensitivity relief tooth | 120 g in 1 TUBE | PASTE, DENTIFRICE | 120 | 1 | |
| 87548-010-02 | Osstem S Sensitivity relief tooth | 1 in 1 CARTON | PASTE, DENTIFRICE | 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.