Home NDC 68599-5501-01 NDC 68599-5501-01 - Antibacterial 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 68599-5501
Requested NDC 68599-5501-01
Package NDCs from labels 68599-5501-1, 68599-5501-2, 68599-5501-3, 68599-5501-4, 68599-5501-01
Manufacturer McKesson | Central Solutions
Effective date 2024-10-11
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 68599-5501-1 Antibacterial 3785 mL in 1 BOTTLE LIQUID 3785 4 68599-5501-2 Antibacterial 1000 mL in 1 BOTTLE LIQUID 1000 4 68599-5501-3 Antibacterial 237 mL in 1 BOTTLE, DISPENSING LIQUID 237 4 68599-5501-4 Antibacterial 532 mL in 1 BOTTLE, DISPENSING LIQUID 532 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68599-5501 ANTIBACTERIAL (BENZETHONIUM CHLORIDE) LIQUID [MCKESSON] 4 Current NDC, Legacy NDC, 4 package rows 20241013_58892abf-e0b9-83d9-e053-2a91aa0ad035.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 47 of 213 · 4,245 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.