Home NDC 10157-9409 NDC 10157-9409 - Blistex Baby Kanka 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 10157-9409
Package NDCs from labels 10157-9409-1
Manufacturer Blistex Inc.
Effective date 2015-01-22
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Blistex Baby Kanka ® Gel Blistex Inc. 2015-01-22 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 10157-9409-1 Blistex Baby Kanka 10 g in 1 TUBE GEL 10 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10157-9409 BLISTEX BABY KANKA (BENZOCAINE) GEL [BLISTEX INC.] 1 1 package rows 20150129_b70ff808-43d3-4a14-867e-b56f9db9da87.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 31 of 55 · 1,083 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.