Aurophen Regular 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: Aurophen Regular Strength
Generic name: ACETAMINOPHEN
Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
SPL set ID: b9b7b849-c3b3-9af7-e053-2a95a90a0077
SPL ID: 0bd1a511-9f43-1a0a-e063-6394a90a10b7
Version: 3
Effective date: 2023-12-06
Source export date: 2026-10-12
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:37:06

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M013	openfda.application_number
brand name		Aurophen Regular Strength	openfda.brand_name
generic name		ACETAMINOPHEN	openfda.generic_name
manufacturer name		KROGER COMPANY	openfda.manufacturer_name
ndc	package	30142-184-21	openfda.package_ndc
ndc	product	30142-184	openfda.product_ndc
ndc11	package	30142018421	derived:openfda.package_ndc
rxcui		313782	openfda.rxcui
spl id		0bd1a511-9f43-1a0a-e063-6394a90a10b7	id
spl set id		b9b7b849-c3b3-9af7-e053-2a95a90a0077	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. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children. Severe liver damage may occur if adult takes more than 4,000 mg of acetaminophen in 24 hours child takes more than 5 doses in 24 hours, which is the maximum daily amount taken with other drugs containing acetaminophen adult has 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.