Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 10361-0793-01 recalled?

E-Z-Gas II · 50 POUCH in 1 BOX (10361-793-01) / 4 g in 1 POUCH

Yes — this exact package was recalled

2 FDA recalls name the code 10361-0793-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Antacid/AntiFlatulent
Strength
ANHYDROUS CITRIC ACID 380 mg/g; SODIUM BICARBONATE 550…
Form
Granule, Effervescent · Oral
Labeler
E-Z-Em, INC.
Type
Human OTC Drug
Product code
10361-0793

Recalls naming this package

Class II · Moderate risk

E-Z-Gas II

cGMP deviations: Temperature abuse

Terminated Temperature excursion Mckesson Medical-Surgical Inc. Corporate Office NDC 0270-9020-01 D-1085-2022

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.