Eyesaline Eyewash Concentrate

Eyesaline Eyewash Concentrate is an FDA-registered drug product whose active ingredient is PURIFIED WATER. It is labelled by Protective Industrial Products, Inc. taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 80716-300, application M018, label effective 20260702. It is one of 7 FDA drug label records sharing the active ingredient PURIFIED WATER. 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.

Across FDA labelling, products containing PURIFIED WATER are most often described in connection with: eye remove, loose foreign, material air, pollutants chlorinated. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For flushing the eye to remove loose foreign material, air pollutants or chlorinated water

Directions Concentrate must be diluted (1) part concentrate to (10) parts potable water before use • Prepare sufficient quantity of constituted eyewash solution in advance of an emergency. • Mix concentrate with potable water to prepare eyewash solution as follows: • Determine quantity of eyewash solution required • Follow sanitary procedures • Wear protective eyewear and gloves • Pour 1/3 of required amount of potable water into mixing container or eyewash unit • Add 1/3 of required amount of concentrate to water • Agitate or mix thoroughly • Repeat until required amount of solution is prepared • Properly dispose of empty bottle after use. • Do not reuse • Keep bottle upright • Replace solution no longer than (6) months after mixing

Warnings For external use only - Obtain immediate medical treatment for all open wounds in or near eyes. To avoid contamination, do not touch tip of container to any surface. Replace cap after use. Do not use In concentrated form While wearing contact lenses For injection In intraocular sugery Internally if eye is lacerated or object is imbeded if seal is broken Stop use and consult a doctor if you have changes in vision continued redness, irritation or pain, or if the condition worsens or persist Keep Out of Reach of Children If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 7 drug label records with PURIFIED WATER as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Eyesaline Eyewash Concentrate used for?
Uses For flushing the eye to remove loose foreign material, air pollutants or chlorinated water

Who makes Eyesaline Eyewash Concentrate?
Protective Industrial Products, Inc. is the labeler of record for Eyesaline Eyewash Concentrate. 7 FDA label records share the active ingredient PURIFIED WATER, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Eyesaline Eyewash Concentrate 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 Eyesaline Eyewash Concentrate 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.

Are there other products containing PURIFIED WATER?
Yes. 7 FDA drug label records list PURIFIED WATER as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Eyesaline Eyewash Concentrate been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

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.