Home NDC 64539-014-01 NDC 64539-014-01 - Folrex Cream 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 64539-014
Requested NDC 64539-014-01
Package NDCs from labels 64539-014-01, 64539-014-02
Manufacturer Catalysis, SL
Effective date 2018-03-09
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Folrex Cream - Catalysis, SL Catalysis, SL 2018-03-09 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 64539-014-01 Folrex Cream 100 mL in 1 TUBE CREAM 100 2 64539-014-02 Folrex Cream 1 in 1 BOX CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64539-014 FOLREX CREAM (MENTHOL) CREAM [CATALYSIS, SL] 2 Legacy NDC, 2 package rows 20180309_6689c713-3731-0760-e053-2a91aa0aca30.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 80 of 387 · 7,740 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.