GEWORIN

GEWORIN is an FDA-registered drug product whose active ingredient is ACETAMINOPHEN, ISOPROPYLANTIPYRINE. It is labelled by Lydia Co., Ltd. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72988-0036, label effective 20230809. 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 ACETAMINOPHEN, ISOPROPYLANTIPYRINE are most often described in connection with: years age, older capsules, three times, day children, ask doctor. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

■ adult and children 15 years of age and older: 1 capsules three times a day ■ children under 15 years of age: ask a doctor

for oral use

Warnings Do not use if carton is open or if printed bottle neck band or inner foil seal is broken.physician Keep out of the reach of children. This package contains enough drug to seriously harm a child. Do not use with other drugs containing acetaminophen. Use the smallest effective dose. Do not take more than the maximum daily dose. Overdose may result in severe or possibly fatal liver damage. Do not take if allergic to acetaminophen. Consult a doctor if: your symptoms last for more than 5 days or fever lasts more than 3 days or you develop allergic reactions such as wheezing, rash or itching. Ask a doctor or pharmacist before use if you: Are pregnant or breastfeeding, have chronic alcoholism; have a serious liver or kidney disease; use any other medications including natural health products, prescription drugs, salicylates or other pain and fever relief medications. In case of overdose, call a Poison Control Centre or doctor immediately, even if you do not notice any possible signs or symptoms such as increased sweating, nausea, vomiting, stomach pain, and loss of appetite.

What is GEWORIN used for?
■ adult and children 15 years of age and older: 1 capsules three times a day ■ children under 15 years of age: ask a doctor

Who makes GEWORIN?
Lydia Co., Ltd. is the labeler of record for GEWORIN.

What form does GEWORIN 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 GEWORIN 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 GEWORIN 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.