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: Bryant Ranch Prepack
Product type: HUMAN OTC DRUG
SPL set ID: 816b65d7-e53f-44c4-a418-074279d4b2af
SPL ID: 7db1fd81-3443-4722-9a1b-497eace4d3c4
Version: 1
Effective date: 2026-05-08
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:55:58

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 · 29 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		Bryant Ranch Prepack	openfda.manufacturer_name
ndc	package	71335-3130-2	openfda.package_ndc
ndc	package	71335-3130-0	openfda.package_ndc
ndc	package	71335-3130-1	openfda.package_ndc
ndc	package	71335-3130-3	openfda.package_ndc
ndc	package	71335-3130-5	openfda.package_ndc
ndc	package	71335-3130-6	openfda.package_ndc
ndc	package	71335-3130-9	openfda.package_ndc
ndc	package	71335-3130-7	openfda.package_ndc
ndc	package	71335-3130-8	openfda.package_ndc
ndc	package	71335-3130-4	openfda.package_ndc
ndc	product	71335-3130	openfda.product_ndc
ndc11	package	71335313006	derived:openfda.package_ndc
ndc11	package	71335313003	derived:openfda.package_ndc
ndc11	package	71335313000	derived:openfda.package_ndc
ndc11	package	71335313001	derived:openfda.package_ndc
ndc11	package	71335313007	derived:openfda.package_ndc
ndc11	package	71335313004	derived:openfda.package_ndc
ndc11	package	71335313005	derived:openfda.package_ndc
ndc11	package	71335313002	derived:openfda.package_ndc
ndc11	package	71335313009	derived:openfda.package_ndc
ndc11	package	71335313008	derived:openfda.package_ndc
rxcui		313782	openfda.rxcui
spl id		7db1fd81-3443-4722-9a1b-497eace4d3c4	id
spl set id		816b65d7-e53f-44c4-a418-074279d4b2af	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 adult takes more than 10 tablets in 24 hours, which is the maximum daily amount child takes more than 5 tablets in 24 hours taken with other drugs containing acetaminophen adult has 3 or more alcoholic drinks every day while using this product

Reported adverse events (FAERS/openFDA)#

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