Euphrasia Officinalis

Euphrasia Officinalis is an FDA-registered drug product whose active ingredient is EUPHRASIA OFFICINALIS. It is labelled by Hahnemann Laboratories, INC. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 37662-0825, label effective 20220712. It is one of 2 FDA drug label records sharing the active ingredient EUPHRASIA OFFICINALIS. 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 EUPHRASIA OFFICINALIS are most often described in connection with: indications condition. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

FDA lists 2 drug label records with EUPHRASIA OFFICINALIS 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 Euphrasia Officinalis used for?
The FDA label on file for this product does not include a full indications section. Other FDA labels sharing the active ingredient EUPHRASIA OFFICINALIS describe it in connection with: indications condition. Check the specific product label or ask a prescriber before use.

Who makes Euphrasia Officinalis?
Hahnemann Laboratories, INC. is the labeler of record for Euphrasia Officinalis. 2 FDA label records share the active ingredient EUPHRASIA OFFICINALIS, 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 Euphrasia Officinalis come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Euphrasia Officinalis 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 EUPHRASIA OFFICINALIS?
Yes. 2 FDA drug label records list EUPHRASIA OFFICINALIS 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 Euphrasia Officinalis 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.