MEDIQUE APAP Extra Strength

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: MEDIQUE APAP Extra Strength
Generic name: ACETAMINOPHEN
Manufacturer: Unifirst First Aid Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 56822785-d5fb-4869-971e-5de637c2eda8
SPL ID: 3e4cc4d7-cd28-c745-e063-6294a90aa614
Version: 20
Effective date: 2025-09-08
Source export date: 2026-10-27
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:14:23

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 · 37 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M013	openfda.application_number
brand name		Medi First Plus Non-Aspirin Extra Strength	openfda.brand_name
brand name		MEDI-FIRST Non-Aspirin Extra Strength	openfda.brand_name
brand name		MEDIQUE APAP Extra Strength	openfda.brand_name
generic name		ACETAMINOPHEN	openfda.generic_name
manufacturer name		Unifirst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-804-13	openfda.package_ndc
ndc	package	47682-804-99	openfda.package_ndc
ndc	package	47682-804-50	openfda.package_ndc
ndc	package	47682-175-99	openfda.package_ndc
ndc	package	47682-175-64	openfda.package_ndc
ndc	package	47682-175-33	openfda.package_ndc
ndc	package	47682-804-48	openfda.package_ndc
ndc	package	47682-175-13	openfda.package_ndc
ndc	package	47682-904-48	openfda.package_ndc
ndc	package	47682-904-33	openfda.package_ndc
ndc	package	47682-804-33	openfda.package_ndc
ndc	package	47682-175-48	openfda.package_ndc
ndc	product	47682-175	openfda.product_ndc
ndc	product	47682-904	openfda.product_ndc
ndc	product	47682-804	openfda.product_ndc
ndc11	package	47682090448	derived:openfda.package_ndc
ndc11	package	47682080450	derived:openfda.package_ndc
ndc11	package	47682017564	derived:openfda.package_ndc
ndc11	package	47682017513	derived:openfda.package_ndc
ndc11	package	47682017599	derived:openfda.package_ndc
ndc11	package	47682080448	derived:openfda.package_ndc
ndc11	package	47682017533	derived:openfda.package_ndc
ndc11	package	47682080499	derived:openfda.package_ndc
ndc11	package	47682017548	derived:openfda.package_ndc
ndc11	package	47682080413	derived:openfda.package_ndc
ndc11	package	47682090433	derived:openfda.package_ndc
ndc11	package	47682080433	derived:openfda.package_ndc
rxcui		198440	openfda.rxcui
spl id		3e4cc4d7-cd28-c745-e063-6294a90aa614	id
spl set id		56822785-d5fb-4869-971e-5de637c2eda8	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 in 24 hours, which is the maximum daily amount 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.