Home NDC 69231-034-01 NDC 69231-034-01 - CLE CCC Golden Medium 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 69231-034
Requested NDC 69231-034-01
Package NDCs from labels 69231-034-01, 69231-034-02
Manufacturer KW ABSC, INC. | Cit Co., Ltd
Effective date 2024-12-19
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 69231-034-01 CLE CCC Golden Medium 30 mL in 1 CONTAINER CREAM 30 2 69231-034-02 CLE CCC Golden Medium 1 in 1 PACKAGE CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69231-034 CLE CCC GOLDEN MEDIUM (TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE) CREAM [KW ABSC, INC.] 2 Current NDC, Legacy NDC, 2 package rows 20241222_de50e956-a014-4147-922b-63c95fa6f86b.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 101 of 620 · 12,400 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.