Rohto Dual Light Relief

Rohto Dual Light Relief is an FDA-registered drug product whose active ingredient is HYPROMELLOSE, POVIDONE. It is labelled by The Mentholatum Company taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 10742-8459, application M018, label effective 20260619. It is one of 2 FDA drug label records sharing the active ingredient HYPROMELLOSE, POVIDONE. 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 HYPROMELLOSE, POVIDONE are most often described in connection with: temporary relief, discomfort due, minor irritations, eye exposure, wind sun, protects against, irritation relieve. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses for the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun protects against further irritation or to relieve dryness of the eye

Directions put 1 or 2 drops in the affected eye(s) as needed tightly snap on cap to seal Other information do not store above 25 O C (77 O F)

Warnings For external use only When using this product do not touch tip of container to any surface to avoid contamination replace cap after each use do not use if solution changes color or becomes cloudy Stop use and ask a doctor if you feel eye pain changes in vision occur redness or irritation of the eyes lasts 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 2 drug label records with HYPROMELLOSE, POVIDONE 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.

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.

What is Rohto Dual Light Relief used for?
Uses for the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun protects against further irritation or to relieve dryness of the eye

Who makes Rohto Dual Light Relief?
The Mentholatum Company is the labeler of record for Rohto Dual Light Relief. 2 FDA label records share the active ingredient HYPROMELLOSE, POVIDONE, 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 Rohto Dual Light Relief 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 Rohto Dual Light Relief 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 HYPROMELLOSE, POVIDONE?
Yes. 2 FDA drug label records list HYPROMELLOSE, POVIDONE 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 Rohto Dual Light Relief 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.