FDA.reportPublic FDA data

MEA protect 75% Alcohol WIPES

Manufacturer
Mid-eastern Advertising
Effective date
2020-11-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:07:15

Label at a glance#

ProductMEA protect 75% Alcohol WIPES
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Store in a cool, dry place.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

75% Ethyl Alcohol

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

decreases bacteria on skin

WARNINGS

WARNINGS SECTION

Highly Flammable liquid and vapor may cause serious eye irritation and if inhaled directly may cause drowsiness or dizziness.

Avoid breathing vapors. If inhaled, move away from the vapors to get fresh air and rest in a comfortable position.

IF EYE CONTACT IS MADE.

Rinse with water for several minutes. If you are wearing contact lenses, remove immediately and continue to rinse.

STORE IN A WELL-VENTILATED PLACE.

CAUTION: Once removed from pack, use immediately to avoid loss of moisture.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF CHILDREN'S REACH.

USAGE:

DOSAGE & ADMINISTRATION SECTION

Open the pack and wipe the desired area with tissue.

STORAGE:

STORAGE AND HANDLING SECTION

Store in a cool, dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Pure Water, 2-Bromo-2-Nitropropane-1.3-Diol, Propylene Glycol, Glycerin, Aloe Vera, Disodium cocoamphodiacetate, PEG 40 Hydrogenated Castor Oil, Phenoxyethanol, Fragrance

SPL UNCLASSIFIED SECTION

CLEANS. SANITIZES. KILLS 99.9% OF GERMS. *

6.0 in x 8.0 in (15 cm x 20 cm)

MADE IN USA

*Germs commonly found on hands. 

PRODUCT CONTENTS: Spunlace Non-woven Fabric, 75% Ethyl Alcohol.

CONTENTS: Multipurpose Alcohol Wipes.

NOT INTENDED FOR MEDICAL USE

MEA MARKETING, LLC.

6741 Whitestone Road

Baltimore, MD 21207

+1 800-833-0044

clientcare@meausa.com

www.MEAUSA.COM

© 2020 MEA Marketing, Inc.

All Rights Reserved.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81041-07581041-075-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
BRONOPOL6PU1E16C9WIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
6c5aede8-d2a5-4a7d-a592-e73d5d5333f557a9141c-6a95-400d-b44b-2cf23b697cc52022-01-17WarningsExact identifier
spl set id: 57a9141c-6a95-400d-b44b-2cf23b697cc5

Reported adverse events (FAERS/openFDA)#

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