acetaminophen

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: acetaminophen
Generic name: ACETAMINOPHEN
Manufacturer: TARGET CORPORATION
Product type: HUMAN OTC DRUG
SPL set ID: 8ed1d1f5-fe4a-5fd8-e053-2a95a90a90fb
SPL ID: 3feb273f-9713-576d-e063-6294a90aaad4
Version: 4
Effective date: 2025-09-29
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:35:02

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M013	openfda.application_number
brand name		acetaminophen	openfda.brand_name
generic name		ACETAMINOPHEN	openfda.generic_name
manufacturer name		TARGET CORPORATION	openfda.manufacturer_name
ndc	package	11673-838-01	openfda.package_ndc
ndc	package	11673-838-10	openfda.package_ndc
ndc	package	11673-838-26	openfda.package_ndc
ndc	package	11673-838-50	openfda.package_ndc
ndc	package	11673-838-05	openfda.package_ndc
ndc	product	11673-838	openfda.product_ndc
ndc11	package	11673083826	derived:openfda.package_ndc
ndc11	package	11673083805	derived:openfda.package_ndc
ndc11	package	11673083810	derived:openfda.package_ndc
ndc11	package	11673083801	derived:openfda.package_ndc
ndc11	package	11673083850	derived:openfda.package_ndc
rxcui		198440	openfda.rxcui
spl id		3feb273f-9713-576d-e063-6294a90aaad4	id
spl set id		8ed1d1f5-fe4a-5fd8-e053-2a95a90a90fb	set_id
unii		362O9ITL9D	openfda.unii

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. Severe liver damage may occur if you take •more than 4,000 mg of acetaminophen in 24 hours •with other drugs containing acetaminophen •3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: •skin reddening •blisters •rash If a skin reaction occurs, stop use and seek medical help right away.

Reported adverse events (FAERS/openFDA)#

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