NDC 81275-014-01 - ROROBELL WAWA Sensitive Teeth 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
- 81275-014
- Requested NDC
- 81275-014-01
- Package NDCs from labels
- 81275-014-01, 81275-014-02
- Manufacturer
- ROROBELL | DONG IL PHARMS CO., LTD.
- Effective date
- 2026-08-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ROROBELL WAWA Sensitive Teeth Tooth - ROROBELL | DONG IL PHARMS CO., LTD. | ROROBELL | DONG IL PHARMS CO., LTD. | 2026-08-04 | HUMAN OTC DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 54c1a27c-5936-4ee2-a419-3891d3df9745 | 2015-08-02 | Warnings, Adverse reactions | 8ZYQ1474W7 RU45X2JN0Z |
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 642fec99-c5c5-4ef2-986e-5b5f7cf460de | 2015-08-02 | Warnings, Adverse reactions | 8ZYQ1474W7 RU45X2JN0Z |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.