Home NDC 71888-101-01 NDC 71888-101-01 - Benzocaine 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 71888-101
Requested NDC 71888-101-01
Package NDCs from labels 71888-101-01, 71888-101-02
Manufacturer Bellus Medical, LLC
Effective date 2026-01-09
Current FDA listing Not matched in FDA.report NDC product tables
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71888-101-01 Benzocaine 4 mL in 1 PACKET GEL 4 4 71888-101-02 Benzocaine 12 in 1 BOX GEL 12 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71888-101 BENZOCAINE GEL [BELLUS MEDICAL, LLC] 3 Current NDC, Legacy NDC, 2 package rows 20241120_60cafbaf-8ec6-46a5-e053-2a91aa0af11f.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 134 of 326 · 6,503 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.