Ripple

Ripple is an FDA-registered drug product whose active ingredient is GLYCERIN, POVIDONE. It is labelled by CorneaCare Inc taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 82875-003, application M018, label effective 20260524. 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 GLYCERIN, POVIDONE are most often described in connection with: temporary relief, irritation due, minor irritations, eye exposure, wind sun, protectant against, relieve dryness. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses • For temporary relief of burning and irritation due to dryness of the eye. • For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun • For use as a protectant against irritation or to relieve dryness of the eye.

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

Warnings For external use only Do not use ■If solution changes color or becomes cloudy. ■lf you are sensitive to any ingredient in this product. When using this product ■Do not touch tip of container to any surface to avoid contamination. ■Replace cap after using. Stop use and ask a doctor if ■You experience eye pain, changes in vision, continued redness or irritation of the eye. ■ Condition worsens or persists for more than 72 hours.

What is Ripple used for?
Uses • For temporary relief of burning and irritation due to dryness of the eye. • For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun • For use as a protectant against irritation or to relieve dryness of the eye.

Who makes Ripple?
CorneaCare Inc is the labeler of record for Ripple.

What form does Ripple 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 Ripple 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 Ripple 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.