Home NDC 71399-8460-05 NDC 71399-8460-05 - OneLAX 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 71399-8460
Requested NDC 71399-8460-05
Package NDCs from labels 71399-8460-2, 71399-8460-5, 71399-8460-05
Manufacturer AKRON PHARMA INC
Effective date 2025-11-03
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type OneLAX - AKRON PHARMA INC AKRON PHARMA INC 2025-11-03 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 71399-8460-2 OneLAX 1 in 1 BLISTER PACK SUPPOSITORY 1 4 71399-8460-2 OneLAX 12 in 1 BOX SUPPOSITORY 12 4 71399-8460-5 OneLAX 50 in 1 BOX SUPPOSITORY 50 4 71399-8460-5 OneLAX 1 in 1 BLISTER PACK SUPPOSITORY 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71399-8460 ONELAX (BISACODYL) SUPPOSITORY [AKRON PHARMA INC] 3 Current NDC, Legacy NDC, 4 package rows 20240922_be4eeb4d-df29-45dc-94ff-933e52c8b6f6.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 1 of 47 · 933 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.