Home NDC 67732-408 NDC 67732-408 - Duane Reade Aloe Vera Pain Relieving 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 67732-408
Package NDCs from labels 67732-408-19
Manufacturer DUANE READE INC.
Effective date 2012-11-14
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Drug Facts DUANE READE INC. 2012-11-14 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 67732-408-19 Duane Reade Aloe VeraPain Relieving 454 g in 1 BOTTLE, PLASTIC GEL 454 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67732-408 DUANE READE ALOE VERA PAIN RELIEVING (LIDOCAINE) GEL [DUANE READE INC.] 1 1 package rows 20121115_d227f447-e129-4c34-8300-d00580e61daa.zip
DailyMed Socrata Ingredients# 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 75 of 178 · 3,544 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.