Home NDC 70738-005-01 NDC 70738-005-01 - Lagom CF Cushion 30 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 70738-005
Requested NDC 70738-005-01
Package NDCs from labels 70738-005-01, 70738-005-02, 70738-005-03, 70738-005-04
Manufacturer SKINMED International Co., Ltd. | Cosmax, Inc.
Effective date 2019-10-23
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type 70738-005_V3 SKINMED International Co., Ltd. | Cosmax, Inc. 2019-10-23 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70738-005-01 Lagom CF Cushion 30 14 g in 1 CONTAINER CREAM 14 3 70738-005-02 Lagom CF Cushion 30 1 in 1 CARTON CREAM 1 3 70738-005-03 Lagom CF Cushion 30 14 g in 1 CONTAINER CREAM 14 3 70738-005-04 Lagom CF Cushion 30 1 in 1 CARTON CREAM 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70738-005 LAGOM CF CUSHION 30 (TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE) CREAM [SKINMED INTERNATIONAL CO., LTD.] 3 Legacy NDC, 4 package rows 20191024_0fa1fb16-0515-4c0d-834d-d932c79ba136.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 180 of 289 · 5,763 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.