ISO-SHIELD Hand Sanitizer

Manufacturer
ESC BRANDS LLC
Effective date
2019-01-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:34:16

Label at a glance#

ProductISO-SHIELD Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use

Dosage and administration

Apply lberally to the palms of the hands.  Rub into skin until dry.  Recocmmended for repeated use.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Antiseptic/Hand & Skin Sanitizer

Uses:

INDICATIONS & USAGE SECTION

Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use

Warnings:

WARNINGS SECTION

Do not freeze, For external use only.

Do nout use 

OTC - DO NOT USE SECTION

in ears, eyes or mouth.

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

OTC - STOP USE SECTION

  • if 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 lberally to the palms of the hands.  Rub into skin until dry.  Recocmmended for repeated use.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

1-octadecyldimethyl (3-triethoxysilylpropyl), Ammonium Chloride, Aloe Barbadenis Leaf Extract, Aqua, C12-C15 Pareth 12, Caprylyl Glucoside, Polyhexanide, Phenoxyethanol, Triethanolamine

Questions?

OTC - QUESTIONS SECTION

+1 (800) 797-1405 Mon-Fri 9:00am-5.00PM (PST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
71884-00571884-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
f8906b3b-0401-49bd-9ff6-95466227a4dc22c7b278-87c5-4cb0-918c-4ddb70973b222021-12-09WarningsExact identifier
spl set id: 22c7b278-87c5-4cb0-918c-4ddb70973b22

Reported adverse events (FAERS/openFDA)#

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