NDC 59368-232 - Walgreens Pain Reliever Extra Strength

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: 59368-232
Package NDCs from labels: 59368-232-03, 59368-232-01, 59368-232-02
Manufacturer: Sixarp, LLC
Effective date: 2025-09-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Walgreens Pain Reliever Extra Strength - Sixarp, LLC	Sixarp, LLC	2025-09-04	HUMAN OTC DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59368-232	WALGREENS PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PRAXIS, LLC]	1	Unmatched	20250223_2ea97514-7ccd-8e41-e063-6294a90aa1a9.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 156 of 156 · 3,102 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SED-MAX	ACETAMINOPHEN 500 MG WITH CAFFEINE 65MG	Command Brands, LLC	4920a0e9-6f88-4df0-8657-77c95a3b9617	2017-01-19	Warnings	Exact identifier unii: 362O9ITL9D
BRONCOCHEM EXPECTORANT II	ACETAMINOPHEN-CHLORPHENIRAMINE MALEATE-DEXTROMETHORPHAN HBR-GUAIFENESIN-PHENYLEPHRINE HCL	LABORATORIO MAGNACHEM INTERNATIONAL SRL	d0426469-9dd1-4bd1-b81e-69d33187daa2	2016-12-19	Warnings	Exact identifier unii: 362O9ITL9D

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.