Duralgina

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Duralgina
Generic name
ACETAMINOPHEN
Manufacturer
Menper Distributors Inc.
Product type
HUMAN OTC DRUG
SPL set ID
bb31f66c-80a9-4bdb-983b-cef5d21de5ff
SPL ID
3a893b13-e7ee-c5b1-e063-6394a90a4253
Version
11
Effective date
2025-07-22
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:58
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: Liver warning: This product contains acetaminophen. Sever liver damage may occur if you take more than12 tablets in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day. Do not use: with any other drug conatining acetaminophen (prescription or non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. If you are allergic to acetaminophen or any of the inactive ingredients in the product. Ask a doctor before use if you have liver disease Ask a docor or pharmacist before use if you are taking the blood thinning drug warfarin Stop using this product and ask a doctor if: Pain gets worse or lasts more than 10 days Fever gets worse or lasts more than 3 days New symptoms occur Redness or swelling is persistent These could be signs of a serious condition

Reported adverse events (FAERS/openFDA)#

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