Aspirin 81 mg

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: Aspirin 81 mg
Generic name: ASPIRIN
Manufacturer: Bryant Ranch Prepack
Product type: HUMAN OTC DRUG
SPL set ID: cce1e8bd-63c8-403a-bc32-e6788493f604
SPL ID: 2e78eab8-ed21-444d-a4bb-21d7929a9760
Version: 104
Effective date: 2025-03-31
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:18:45

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M013	openfda.application_number
brand name		Aspirin 81 mg	openfda.brand_name
generic name		ASPIRIN	openfda.generic_name
manufacturer name		Bryant Ranch Prepack	openfda.manufacturer_name
ndc	package	71335-1774-4	openfda.package_ndc
ndc	package	71335-1774-1	openfda.package_ndc
ndc	package	71335-1774-6	openfda.package_ndc
ndc	package	71335-1774-5	openfda.package_ndc
ndc	package	71335-1774-8	openfda.package_ndc
ndc	package	71335-1774-2	openfda.package_ndc
ndc	package	71335-1774-3	openfda.package_ndc
ndc	package	71335-1774-7	openfda.package_ndc
ndc	product	71335-1774	openfda.product_ndc
ndc11	package	71335177405	derived:openfda.package_ndc
ndc11	package	71335177406	derived:openfda.package_ndc
ndc11	package	71335177403	derived:openfda.package_ndc
ndc11	package	71335177401	derived:openfda.package_ndc
ndc11	package	71335177407	derived:openfda.package_ndc
ndc11	package	71335177408	derived:openfda.package_ndc
ndc11	package	71335177402	derived:openfda.package_ndc
ndc11	package	71335177404	derived:openfda.package_ndc
rxcui		308416	openfda.rxcui
spl id		2e78eab8-ed21-444d-a4bb-21d7929a9760	id
spl set id		cce1e8bd-63c8-403a-bc32-e6788493f604	set_id
unii		R16CO5Y76E	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 Reye's syndrome: Children and teenagers who have or are recoving from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be early sign of Reye's syndrome, a rare but serious illness.

Reported adverse events (FAERS/openFDA)#

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