Neutraflush

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: Neutraflush
Generic name: EYEWASH STATION ADDITIVE CONCENTRATE
Manufacturer: Aero Healthcare
Product type: HUMAN OTC DRUG
SPL set ID: 1d9ff2ef-9c9b-f367-e063-6294a90afa0e
SPL ID: 576246c7-981f-d279-e063-6294a90a4e45
Version: 3
Effective date: 2026-07-24
Source export date: 2026-10-27
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:45:38

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Neutraflush	openfda.brand_name
generic name		EYEWASH STATION ADDITIVE CONCENTRATE	openfda.generic_name
manufacturer name		Aero Healthcare	openfda.manufacturer_name
ndc	package	55305-134-01	openfda.package_ndc
ndc	product	55305-134	openfda.product_ndc
ndc11	package	55305013401	derived:openfda.package_ndc
spl id		576246c7-981f-d279-e063-6294a90a4e45	id
spl set id		1d9ff2ef-9c9b-f367-e063-6294a90afa0e	set_id
unii		6DC9Q167V3	openfda.unii
unii		MOR84MUD8E	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. In case of contact with eye in undiluted form, flush with clean water Do not use in full strength When using this product do not change dilution or use with other chemicals do not reuse 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 irritations of the eye

Reported adverse events (FAERS/openFDA)#

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