GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg

ESOMEPRAZOLE MAGNESIUM 20MG ORAL HUMAN OTC DRUG

GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg is an FDA drug label for the active ingredient ESOMEPRAZOLE MAGNESIUM 20MG manufactured by Cabinet Health P.B.C. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260811.

Generic name
ESOMEPRAZOLE MAGNESIUM 20MG
Manufacturer
Cabinet Health P.B.C.
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
82725-4053
Application
ANDA212507
Label effective
20260811

About this product

GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg is an FDA-registered drug product whose active ingredient is ESOMEPRAZOLE MAGNESIUM 20MG. It is labelled by Cabinet Health P.B.C. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 82725-4053, application ANDA212507, label effective 20260811. 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.

What it is used for

Across FDA labelling, products containing ESOMEPRAZOLE MAGNESIUM 20MG are most often described in connection with: treats frequent, heartburn occurs, days week, immediate relief, full effect. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Esomeprazole 20 mg (*Each delayed-release capsule corresponds to 22.25 mg esomeprazole magnesium trihydrate USP)

Indications & Usage

Uses  treats frequent heartburn (occurs 2 or more days a week)  not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect.

Dosage & Administration

Directions  adults 18 years of age and older  this product is to be used once a day (every 24 hours), every day for 14 days  may take 1 to 4 days for full effect 14-Day Course of Treatment  swallow 1 capsule with a glass of water before eating in the morning  take every day for 14 days  do not take more than 1 capsule a day  swallow whole. Do not crush or chew capsules.  do not use for more than 14 days unless directed by your doctor Repeated 14-Day Courses (if needed)  you may repeat a 14-day course every 4 months  do not take for more than 14 days or more often than every 4 months unless directed by a doctor  children under 18 years of age: ask a doctor before use. Heartburn in children may sometimes be caused by a serious condition.

Warnings

Warnings Allergy alert:  Do not use if you are allergic to esomeprazole.  Esomeprazole may cause severe skin reactions. Symptoms may include:  skin reddening  blisters  rash If an allergic reaction occurs, stop use and seek medical help right away.

Frequently asked questions

What is GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg used for?
Uses  treats frequent heartburn (occurs 2 or more days a week)  not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect.

Who makes GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg?
Cabinet Health P.B.C. is the labeler of record for GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg.

What form does GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg 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 GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg 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 GoodMeds Acid Reducer 24HR Esomeprazole Magnesium Delayed-Release 20mg 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.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.