Neutraflush

EYEWASH STATION ADDITIVE CONCENTRATE OPHTHALMIC HUMAN OTC DRUG

Neutraflush is an FDA drug label for the active ingredient EYEWASH STATION ADDITIVE CONCENTRATE manufactured by Aero Healthcare administered by OPHTHALMIC. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260724.

Generic name
EYEWASH STATION ADDITIVE CONCENTRATE
Manufacturer
Aero Healthcare
Product type
HUMAN OTC DRUG
Route
OPHTHALMIC
Dosage form
N/A
NDC
55305-134
Application
M018
Label effective
20260724

About this product

Neutraflush is an FDA-registered drug product whose active ingredient is EYEWASH STATION ADDITIVE CONCENTRATE. It is labelled by Aero Healthcare taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 55305-134, application M018, label effective 20260724. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing EYEWASH STATION ADDITIVE CONCENTRATE are most often described in connection with: potable self-contained, emergency eyewash. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Ingredients Chlorhexidine gluconate 1% w/v Purified Water, Propylene Glycol

Indications & Usage

Use A preservative for use in potable self-contained emergency eyewash stations

Dosage & Administration

Directions wear protective eyewear and gloves clean potable eyewash station and rinse with potable water partially fill station with potable water remove tamper evident seal and cap of bottle add entire contents of the bottle to the eyewash station container fill the station to the manufacturer's required level date and initial inspection tag station should be cleaned and refilled every 120 days when using this product in advance of emergency, add the concentrate to potable water to have solution available

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

Recall and safety notices

1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-0155-2026 Acetaminophen 500mg Caffeine 65mg caplets, packaged as 2 caplets per packet further packaged in a 50-count box, AERO TAB, Manufactured for AERO HEALTHCARE US, Valley-Cottage, NY, 10989, NDC 55305-135-01 Aero Healthcare Class II Ongoing 20251112

Frequently asked questions

What is Neutraflush used for?
Use A preservative for use in potable self-contained emergency eyewash stations

Who makes Neutraflush?
Aero Healthcare is the labeler of record for Neutraflush.

What form does Neutraflush come in?
administered by ophthalmic. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Neutraflush prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Neutraflush been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.