Fendall 1000 Pure Flow

Fendall 1000 Pure Flow 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 80716-100, 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: flushing irrigating, eye reduce, chances severe, injury caused, acid alkali, particulate contamination. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination.

Directions pull handle on the activating door to initiate flow lower head into flow for 15 minutes if necessary, continue flushing with emergency eyewash or shower do not reuse discard cartridge after use

Warnings For external use only Do not use If solution changes color or gets cloudy In open wounds in or near the eyes with contact lenses Stop use and ask a doctor if you have changes in vision eye pain continued redness, irritation of the eye or if the condition worsens or persists. 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 Fendall 1000 Pure Flow used for?
Uses For flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination.

Who makes Fendall 1000 Pure Flow?
Protective Industrial Products, Inc. is the labeler of record for Fendall 1000 Pure Flow. 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 Fendall 1000 Pure Flow 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 Fendall 1000 Pure Flow 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 Fendall 1000 Pure Flow 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.