My-Shield Hand Sanitizer

Manufacturer
Enviro Specialty Chemicals Inc
Effective date
2021-10-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:33:52

Label at a glance#

ProductMy-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 liberally to the palms of the hands. Rub into skin until dry. Recommended for repeat 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 not use 

OTC - DO NOT USE SECTION

in ears 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 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 liberally to the palms of the hands. Rub into skin until dry. Recommended for repeat use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

1-Octadecanaminium NN dimethyl (3-trimethoxysilyl) propyl chloride, 1-Octadecanaminium NN dimethyl (3-trihydroxysilyl) propyl chloride, Aloe Barbadenis leaf extract, Aqua, Caprylyl Glucoside, Citric Acid, laureth-4, Methyl Parabens, Polyaminopropyl biguanide, Silk Protein.

Questions?

OTC - QUESTIONS SECTION

+1 (336) 655 2219 Mon-Fri 9:00AM-5:00PM (EST)

Packgae Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71884-00271884-002-01, 71884-002-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
cdc46386-c3c7-db30-e053-2a95a90a1fcb84fd6ef3-6293-447c-a6bf-c344ec171adf2021-10-07WarningsExact identifier
spl id: cdc46386-c3c7-db30-e053-2a95a90a1fcb
spl set id: 84fd6ef3-6293-447c-a6bf-c344ec171adf

Reported adverse events (FAERS/openFDA)#

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