Aluminum Hydroxide, Magnesium Hydroxide and Simethicone

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Aluminum Hydroxide, Magnesium Hydroxide and Simethicone
Generic name: ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE
Manufacturer: Everpharm LLC
Product type: HUMAN OTC DRUG
SPL set ID: 2bda74cb-e77d-46bb-e063-6394a90af580
SPL ID: 2bda8639-5512-d3fd-e063-6294a90a04ee
Version: 1
Effective date: 2025-01-16
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:37:51

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
application number		M001.15	openfda.application_number
brand name		Aluminum Hydroxide, Magnesium Hydroxide and Simethicone	openfda.brand_name
generic name		ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE	openfda.generic_name
manufacturer name		Everpharm LLC	openfda.manufacturer_name
ndc	package	84415-010-01	openfda.package_ndc
ndc	package	84415-017-01	openfda.package_ndc
ndc	product	84415-010	openfda.product_ndc
ndc	product	84415-017	openfda.product_ndc
ndc11	package	84415001701	derived:openfda.package_ndc
ndc11	package	84415001001	derived:openfda.package_ndc
rxcui		237870	openfda.rxcui
rxcui		307746	openfda.rxcui
spl id		2bda8639-5512-d3fd-e063-6294a90a04ee	id
spl set id		2bda74cb-e77d-46bb-e063-6394a90af580	set_id
unii		5QB0T2IUN0	openfda.unii
unii		NBZ3QY004S	openfda.unii
unii		92RU3N3Y1O	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Ask a doctor before use if you have • kidney disease • a magnesium restricted diet Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs Stop use and ask a doctor if symptoms last more than 2 weeks If pregnant or breast-feeding, ask a healthcare professional before use Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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