Home NDC 71702-090-01 NDC 71702-090-01 - CLEMATIS Morning dew BB 21 Light Beige 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 71702-090
Requested NDC 71702-090-01
Package NDCs from labels 71702-090-01, 71702-090-02
Manufacturer Coshub Co., Ltd. | COSON Co., Ltd._Osan Plant
Effective date 2017-09-05
Current FDA listing Not matched in FDA.report NDC product tables
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71702-090-01 CLEMATIS Morning dew BB 21 Light Beige 50 mL in 1 TUBE CREAM 50 1 71702-090-02 CLEMATIS Morning dew BB 21 Light Beige 1 in 1 CARTON CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71702-090 CLEMATIS MORNING DEW BB 21 LIGHT BEIGE (TITANIUM DIOXIDE) CREAM [COSHUB CO., LTD.] 1 Legacy NDC, 2 package rows 20170905_d4563e37-8cfa-4e77-83da-64118f9912c0.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 89 of 277 · 5,536 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.