Home NDC 81275-010-01 NDC 81275-010-01 - Rorobell WaWa 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 81275-010
Requested NDC 81275-010-01
Package NDCs from labels 81275-010-01, 81275-010-02
Manufacturer ROROBELL | DONG IL PHARMS CO., LTD.
Effective date 2026-08-03
Current FDA listing Not matched in FDA.report NDC product tables
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81275-010-01 Rorobell WaWa Tooth 100 g in 1 TUBE PASTE, DENTIFRICE 100 4 81275-010-02 Rorobell WaWa Tooth 1 in 1 CARTON PASTE, DENTIFRICE 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81275-010 ROROBELL WAWA TOOTH (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [ROROBELL] 3 Current NDC, Legacy NDC, 2 package rows 20241210_93113481-ad9d-4be0-a7b7-a72c8726127d.zip
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.
Matched openFDA labels page 91 of 99 · 1,968 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.