BRIZZEL

Manufacturer
MAGS CHEM CORP
Effective date
2020-10-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:11

Label at a glance#

ProductBRIZZEL
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

ANTIBACTERIAL.

Dosage and administration

FOR PERSONAL AND HOME USE, APPLY ON HANDS

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 75%

Purpose

OTC - PURPOSE SECTION

ANTIBACTERIAL

Warnings

WARNINGS SECTION

MAY BE FLAMABLE

KEEP OUT OF REACH OF CHILDREN

DO NOT INGEST

IN CASE OF IRRITATION USE WATER, GET MEDICAL HELP

Uses

INDICATIONS & USAGE SECTION

ANTIBACTERIAL.

Directions

DOSAGE & ADMINISTRATION SECTION

FOR PERSONAL AND HOME USE, APPLY ON HANDS

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER,ALOE VERA,BENZETHONIUM CHLORIDE.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80303-001-012022-01-28C16284748780-1d6a99b39-6418-a426-e053-dadaa90af4c2BRIZZEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80303-001-01BRIZZEL100 in 1 CANISTERCLOTH1001
80303-001-01BRIZZEL2.82 mL in 1 NOT APPLICABLECLOTH2.821

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80303-001BRIZZEL (ALCOHOL) CLOTH [MAGS CHEM CORP]1Legacy NDC, 2 package rows20201022_105d2c51-e8bc-418a-aacf-626f8f697a31.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80303-00180303-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e9ae269b-a5ab-46dd-8a54-9f6608fb54f5105d2c51-e8bc-418a-aacf-626f8f697a312020-10-13WarningsExact identifier
spl id: e9ae269b-a5ab-46dd-8a54-9f6608fb54f5
spl set id: 105d2c51-e8bc-418a-aacf-626f8f697a31

Reported adverse events (FAERS/openFDA)#

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