FDA.reportPublic FDA data

Ecoshield Skin Advanced Antimicrobial Hand Sanitizer

Manufacturer
Matrix Antimicrobial, LLC
Effective date
2022-10-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:50:58

Label at a glance#

ProductEcoshield Skin Advanced Antimicrobial Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Hand sanitizer to help kill 99.9% of germs. Recommended for repeated use.

Dosage and administration

Apply a small amount into palms of hands and spread on both hands. Rub into skin until dry. To maintain maximum effectiveness, apply to clean dry hands every 6 to 8 hours.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help kill 99.9% of germs.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • in ears or mouth and avoid mucus membranes.

When using this product.

OTC - WHEN USING SECTION

  • Avoid contact with the eyes.
  • In case of contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children should be supervised when using this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a small amount into palms of hands and spread on both hands.
  • Rub into skin until dry.
  • To maintain maximum effectiveness, apply to clean dry hands every 6 to 8 hours.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, 3-(Trimethoxy) Propyl Dimethyl Octadecyl Ammonium Chloride, ethoxylated alcohol, Citrus Limon (Lemon) Fruit Oil.

Package Labeling:81499-001-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:81499-001-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81499-00181499-001-01, 81499-001-02

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CITRUS X LIMON FRUIT OIL0HNC1J1YEDIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDEIQ36O85WQ4IACT

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
ebd50de1-c84f-95e5-e053-2a95a90aa96cba84127e-dbc1-4645-e053-2a95a90a76f82022-10-25WarningsExact identifier
spl id: ebd50de1-c84f-95e5-e053-2a95a90aa96c
spl set id: ba84127e-dbc1-4645-e053-2a95a90a76f8

Reported adverse events (FAERS/openFDA)#

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