Home NDC 73676-217-01 NDC 73676-217-01 - Abib Heartleaf mild sunscreen Relief tube 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 73676-217
Requested NDC 73676-217-01
Package NDCs from labels 73676-217-01, 73676-217-02
Manufacturer FOURCOMPANY CO., LTD. | Cosmax, Inc.
Effective date 2025-05-07
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 73676-217-01 Abib Heartleaf mild sunscreen Relief tube 50 mL in 1 TUBE CREAM 50 1 73676-217-02 Abib Heartleaf mild sunscreen Relief tube 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 73676-217 ABIB HEARTLEAF MILD SUNSCREEN RELIEF TUBE (ZINC OXIDE) CREAM [FOURCOMPANY CO., LTD.] 1 Current NDC, 2 package rows 20250509_34965587-c9b7-4066-e063-6394a90ab424.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 37 of 445 · 8,891 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.