E-Z-GAS II

ANTACID/ANTIFLATULENT ORAL HUMAN OTC DRUG

E-Z-GAS II is an FDA drug label for the active ingredient ANTACID/ANTIFLATULENT manufactured by E-Z-EM, INC. 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 20260615.

Generic name
ANTACID/ANTIFLATULENT
Manufacturer
E-Z-EM, INC.
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
10361-793
Application
M001
Label effective
20260615

About this product

E-Z-GAS II is an FDA-registered drug product whose active ingredient is ANTACID/ANTIFLATULENT. It is labelled by E-Z-EM, INC. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 10361-793, application M001, label effective 20260615. 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.

Active ingredients

Once package is opened, discard unused portion.

Dosage & Administration

Directions Recommended dose Maximum recommended dose Adults (under 60 years) One packet every 6 hours or as directed by physician Not to exceed 4 packets in 24 hours Adults (60 years and older) One packet every 8 hours or as directed by physician Not to exceed 3 packets in 24 hours Children (6 to 12 years) One packet every 8 hours or as directed by physician Not to exceed 3 packets in 24 hours Children Under 6 years Consult physician Consult physician

Warnings

Warnings

Recall and safety notices

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.

RecallProductFirmClassStatusReported
D-1085-2022 E-Z-Gas II, Effervescent Granules, Net Weight: 4 g, 50 packets per box, MFG: Bracco Diagnostics Inc., NDC 0270-9020-01 (discontinued), NDC 10361-793-01 (current) Mckesson Medical-Surgical Inc. Corporate Office Class II Terminated 20220615

Frequently asked questions

What is E-Z-GAS II used for?
No indications section is present in the FDA label on file for this product. Consult the prescribing information supplied with the medicine or ask a pharmacist.

Who makes E-Z-GAS II?
E-Z-EM, INC. is the labeler of record for E-Z-GAS II.

What form does E-Z-GAS II 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 E-Z-GAS II 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 E-Z-GAS II 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.

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.