NDC 79481-0638-01 - Maximum Strength Antacid and Antigas

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 79481-0638
Requested NDC: 79481-0638-01
Package NDCs from labels: 79481-0638-1, 79481-0638-01
Manufacturer: Meijer, Inc. | GCP Laboratories
Effective date: 2025-07-30
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Maximum Strength Antacid and Antigas - Meijer, Inc. \| GCP Laboratories	Meijer, Inc. \| GCP Laboratories	2025-07-30	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79481-0638-1	Maximum Strength Antacid and Antigas	355 mL in 1 BOTTLE	SUSPENSION	355		2

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 82 of 82 · 1,624 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ARGAN AIR WATER BANG ESSENCE	DIMETHICONE	Pioom Cosmetic Co.,ltd	34e79668-0710-5753-e054-00144ff88e88	2016-06-08	Warnings	Exact identifier unii: 92RU3N3Y1O
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Antacid	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE AND SIMETHICONE	Safeway	d36b56a4-06f0-47ff-8add-4c327d60be22	2016-01-21	Warnings	Exact identifier rxcui: 237870 unii: 5QB0T2IUN0 unii: NBZ3QY004S unii: 92RU3N3Y1O
Gas Relief	SIMETHICONE	Safeway	14a9fb00-707a-4b55-a060-82ad53a806e3	2016-01-08	Warnings	Exact identifier unii: 92RU3N3Y1O

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.