MiraFAST soft chews

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: MiraFAST soft chews
Generic name: MAGNESIUM HYDROXIDE
Manufacturer: Bayer HealthCare LLC.
Product type: HUMAN OTC DRUG
SPL set ID: 2cee67dd-b71f-32b8-e063-6394a90ae864
SPL ID: 59911b66-9545-f86c-e063-6394a90a3eab
Version: 3
Effective date: 2026-08-21
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:13:38

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		M007	openfda.application_number
brand name		MiraFAST soft chews	openfda.brand_name
generic name		MAGNESIUM HYDROXIDE	openfda.generic_name
manufacturer name		Bayer HealthCare LLC.	openfda.manufacturer_name
ndc	package	11523-0159-1	openfda.package_ndc
ndc	package	11523-0159-4	openfda.package_ndc
ndc	package	11523-0159-2	openfda.package_ndc
ndc	package	11523-0159-3	openfda.package_ndc
ndc	product	11523-0159	openfda.product_ndc
ndc11	package	11523015901	derived:openfda.package_ndc
ndc11	package	11523015903	derived:openfda.package_ndc
ndc11	package	11523015904	derived:openfda.package_ndc
ndc11	package	11523015902	derived:openfda.package_ndc
rxcui		2280709	openfda.rxcui
rxcui		2705611	openfda.rxcui
spl id		59911b66-9545-f86c-e063-6394a90a3eab	id
spl set id		2cee67dd-b71f-32b8-e063-6394a90ae864	set_id
unii		NBZ3QY004S	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 Do not use Do not use if you have ever had an allergic reaction to this product or any of its ingredients Ask a doctor before use if you have Ask a doctor before use if you have kidney disease a magnesium-restricted diet stomach pain, nausea, or vomiting a sudden change in bowel habits that lasts over 14 days Ask a doctor or pharmacist before use if you are Ask a doctor or pharmacist before use if you are taking a prescription drug. This product may interact with certain prescription drugs. Stop use and ask a doctor Stop use and ask a doctor if you have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition. you need to use a laxative for more than 1 week

Reported adverse events (FAERS/openFDA)#

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