AeroWash Eyewash

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: AeroWash Eyewash
Generic name: EYEWASH SOLUTION
Manufacturer: Aero Healthcare US LLC
Product type: HUMAN OTC DRUG
SPL set ID: a477de08-4301-0ee5-e053-2995a90af79d
SPL ID: 2f179d38-236f-6d3f-e063-6294a90a6867
Version: 3
Effective date: 2025-02-26
Source export date: 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:56

Harmonized routes table
Harmonized routes
OPHTHALMIC

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	022305	derived:openfda.application_number
application number		NDA022305	openfda.application_number
brand name		AeroWash Eyewash	openfda.brand_name
generic name		EYEWASH SOLUTION	openfda.generic_name
manufacturer name		Aero Healthcare US LLC	openfda.manufacturer_name
ndc	package	55305-115-10	openfda.package_ndc
ndc	package	55305-115-13	openfda.package_ndc
ndc	package	55305-115-12	openfda.package_ndc
ndc	package	55305-115-11	openfda.package_ndc
ndc	product	55305-115	openfda.product_ndc
ndc11	package	55305011512	derived:openfda.package_ndc
ndc11	package	55305011511	derived:openfda.package_ndc
ndc11	package	55305011510	derived:openfda.package_ndc
ndc11	package	55305011513	derived:openfda.package_ndc
rxcui		1151101	openfda.rxcui
spl id		2f179d38-236f-6d3f-e063-6294a90a6867	id
spl set id		a477de08-4301-0ee5-e053-2995a90af79d	set_id
unii		059QF0KO0R	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 For external use only Do not use if you experience any open wounds in or near the eyes and obtain immediate medical treatment if solution changes color or becomes cloudy When using this product to avoid contamination, do not touch tip of container to any surface do not reuse once opened, discard Stop use and ask a doctor if you have any of the following changes in vision eye pain condition worsens or persists continued redness or irritation of the eye

Reported adverse events (FAERS/openFDA)#

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