My-Shield Topical Antiseptic

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 22:33:49

Label at a glance#

ProductMy-Shield Topical Antiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

First aid soothing and germ protection for: • minor cuts • abrasions • pressure sores • sunburn • scrapes • burns • skin irritations

Dosage and administration

Apply liberally over effected area, recommended for repeat application regularly.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic - Topical skin treatment

Uses

INDICATIONS & USAGE SECTION

  • First aid soothing and germ protection for: • minor cuts • abrasions • pressure sores • sunburn • scrapes • burns • skin irritations

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 over effected area, recommended for repeat application regularly.

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, Hydroxyethyl cellulose, laureth-4, Methyl Parabens, Polyaminopropyl biguanide, Silk Protein.

Questions?

OTC - QUESTIONS SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

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
71884-00171884-001-02, 71884-001-04, 71884-001-06

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-c3c9-db30-e053-2a95a90a1fcb54670ae2-68cd-49a8-9b79-b5a759c0cec12021-10-07WarningsExact identifier
spl id: cdc46386-c3c9-db30-e053-2a95a90a1fcb
spl set id: 54670ae2-68cd-49a8-9b79-b5a759c0cec1

Reported adverse events (FAERS/openFDA)#

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