GILTUSS DIABETIC EX

GILTUSS DIABETIC EX is an FDA-registered drug product whose active ingredient is GILTUSS DIABETIC EX. It is labelled by Gil Pharmaceutical Corp taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 58552-339, application M012, label effective 20260513. 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 GILTUSS DIABETIC EX are most often described in connection with: helps loosen, phlegm mucus, thin bronchial, secretions rid, passageways bothersome, make cough. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and helps make cough more productive.

Directions do not crush, chew, or break tablet take with a full glass of water this product can be administered without regard for the timing of meals adults and children 12 years of age and over: 1 or 2 tablets every 12 hours do not exceed 4 tablets in 24 hours children under 12 years of age: do not use

Warnings Do not use for children under 12 years

What is GILTUSS DIABETIC EX used for?
Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and helps make cough more productive.

Who makes GILTUSS DIABETIC EX?
Gil Pharmaceutical Corp is the labeler of record for GILTUSS DIABETIC EX.

What form does GILTUSS DIABETIC EX 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 GILTUSS DIABETIC EX 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 GILTUSS DIABETIC EX 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.