MEDIQUE Diamode

MEDIQUE Diamode is an FDA-registered drug product whose active ingredient is LOPERAMIDE HYDROCHLORIDE. It is labelled by Sportpharm LLC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 85766-120, application ANDA074091, label effective 20260424. It is one of 53 FDA drug label records sharing the active ingredient LOPERAMIDE HYDROCHLORIDE. 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 LOPERAMIDE HYDROCHLORIDE are most often described in connection with: symptoms diarrhea, including travelers. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Controls the symptoms of diarrhea, including Travelers diarrhea.

Directions do not use more than directed drink plenty of clear fluids to help prevent dehydration caused by diarrhea Adults and children (12 years and older): Take 2 caplets after the first loose stool followed by 1 caplet after each subsequent loose stool but no more than 4 caplets in 24 hours. Children under 12 years: Do not give to children under 12 years of age.

Warnings Allergy alert: Do not use if you have ever had a rash or other allergic reaction to Loperamide HCl Do not use if you have bloody or black stool Ask a doctor before use if you have a fever mucus in stool a history of liver disease Ask a doctor or pharmacist before use if you are taking antibiotics When using this product tiredness, drowsiness or dizziness may occur be careful when driving or operating machinery Stop use and ask a doctor if symptoms get worse diarrhea lasts more than 2 days you get abdominal swelling or bulging. These may be signs of a serious condition. If you are pregnant or breast feeding , ask a health professional before use. Keep this and all drugs out of the reach of children . In case of accidental overdose, contact a physician or Poison Control Center right away.

FDA lists 53 drug label records with LOPERAMIDE HYDROCHLORIDE 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 MEDIQUE Diamode used for?
Uses Controls the symptoms of diarrhea, including Travelers diarrhea.

Who makes MEDIQUE Diamode?
Sportpharm LLC is the labeler of record for MEDIQUE Diamode. 53 FDA label records share the active ingredient LOPERAMIDE HYDROCHLORIDE, 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 MEDIQUE Diamode 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 MEDIQUE Diamode 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 LOPERAMIDE HYDROCHLORIDE?
Yes. 53 FDA drug label records list LOPERAMIDE HYDROCHLORIDE 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 MEDIQUE Diamode 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.