REFRESH LIQUIGEL

REFRESH LIQUIGEL is an FDA-registered drug product whose active ingredient is CARBOXYMETHYLCELLULOSE SODIUM. It is labelled by Allergan, Inc. taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 0023-9205, application M018, label effective 20260828. It is one of 17 FDA drug label records sharing the active ingredient CARBOXYMETHYLCELLULOSE SODIUM. 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 CARBOXYMETHYLCELLULOSE SODIUM are most often described in connection with: temporary relief, burning irritation, discomfort due, eye exposure, wind sun, protectant against. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. May be used as a protectant against further irritation.

Directions Instill 1 or 2 drops in the affected eye(s) as needed.

Warnings For external use only. To avoid contamination, do not touch tip of container to any surface. Replace cap after using. If solution changes color or becomes cloudy , do not use. Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 17 drug label records with CARBOXYMETHYLCELLULOSE SODIUM 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 REFRESH LIQUIGEL used for?
Uses For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. May be used as a protectant against further irritation.

Who makes REFRESH LIQUIGEL?
Allergan, Inc. is the labeler of record for REFRESH LIQUIGEL. 17 FDA label records share the active ingredient CARBOXYMETHYLCELLULOSE SODIUM, 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 REFRESH LIQUIGEL 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 REFRESH LIQUIGEL 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 CARBOXYMETHYLCELLULOSE SODIUM?
Yes. 17 FDA drug label records list CARBOXYMETHYLCELLULOSE SODIUM 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 REFRESH LIQUIGEL 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.