Home NDC 83024-002-01 NDC 83024-002-01 - LAUNDRYOU CLEAR DEFENSE CUSHION GLOW 21 UYUNI 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 83024-002
Requested NDC 83024-002-01
Package NDCs from labels 83024-002-01, 83024-002-02
Manufacturer bvmt Co.,Ltd. | Cosmax, Inc.
Effective date 2022-10-05
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 83024-002-01 LAUNDRYOU CLEAR DEFENSE CUSHION GLOW 21 UYUNI BEIGE 13 g in 1 CONTAINER CREAM 13 1 83024-002-02 LAUNDRYOU CLEAR DEFENSE CUSHION GLOW 21 UYUNI 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 83024-002 LAUNDRYOU CLEAR DEFENSE CUSHION GLOW 21 UYUNI BEIGE (OCTINOXATE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE) CREAM [BVMT CO.,LTD.] 1 Legacy NDC, 2 package rows 20221007_fc03eb47-63d2-4777-a165-eeab0e24561d.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 40 of 482 · 9,626 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.