Home NDC 72249-001 NDC 72249-001 - Dandrene 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 72249-001
Package NDCs from labels 72249-001-01
Manufacturer Divine Skin Laboratories S.A. de C.V. | A.I.G. Technologies, Inc.
Effective date 2020-11-30
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Dandrene Conditioner Divine Skin Laboratories S.A. de C.V. | A.I.G. Technologies, Inc. 2020-11-30 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 72249-001-01 Dandrene 1 in 1 BOX LOTION 1 2 72249-001-01 Dandrene 205 g in 1 BOTTLE LOTION 205 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72249-001 DANDRENE (PYRITHIONE ZINC) LOTION [DIVINE SKIN LABORATORIES S.A. DE C.V.] 2 2 package rows 20201201_615f5a14-50bb-493e-a441-5afcf62e8498.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 26 of 277 · 5,522 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.