FDA.reportPublic FDA data

MY-SHIELD SANITIZING BODY SPRAY

Manufacturer
Enviro Specialty Chemicals Inc
Effective date
2026-01-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:48:06

Label at a glance#

ProductMy-Shield Sanitizing Body
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

First aid anti-microbial - Topical body sanitizer • Preventive antiseptic

Dosage and administration

Spray liberally over the entire body and personal clothing, recommended for repeat application regularly, product safe on all surfaces & fabric’s.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

First aid anti-microbial - Topical body sanitizer • Preventive antiseptic

Directions:

DOSAGE & ADMINISTRATION SECTION

Spray liberally over the entire body and personal clothing, recommended for repeat application regularly, product safe on all surfaces & fabric’s.

Warnings:

WARNINGS SECTION

Do not freeze. For external use only.

Do not use in ears, eyes or mouth.

• When using this product, avoid contact with the eyes. In case of contact, flush eyes with water.

• Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Deceth-6, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Questions?

OTC - QUESTIONS SECTION

+1(888) 331-8332, M-F, 9AM-5PM (EST)

SPL UNCLASSIFIED SECTION

FAST ACTING 15 SECOND FORMULA

WITH SOOTHING ALOE VERA

Alcohol-Free

Long lasting, sanitizing protection from germs for the entire body

KILLS 99.99% OF GERMS

Formulated and enhanced with Zetrisil​® ​​

MADE IN THE USA

Distributed by: ESC Brands, LLC.
1026 Blue Prince Road, suite B
Bluefield, WV 24701
www.escbrands.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

My-Shield Sanitizing BodyMy-Shield Sanitizing Body

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1052947benzalkonium chloride 0.1 % Topical SprayPSN3
1052947benzalkonium chloride 1 MG/ML Topical SpraySCD3
1052947benzalkonium chloride 0.1 % Topical SpraySY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71884-009-01My-Shield Sanitizing Body50 mL in 1 BOTTLE, SPRAYSPRAY503
71884-009-02My-Shield Sanitizing Body58 mL in 1 BOTTLE, SPRAYSPRAY583
71884-009-05My-Shield Sanitizing Body3785 mL in 1 BOTTLE, SPRAYSPRAY37853
71884-009-16My-Shield Sanitizing Body473 mL in 1 BOTTLE, SPRAYSPRAY4733

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71884-00971884-009-02, 71884-009-16, 71884-009-01, 71884-009-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
DECETH-6P4OYN7A2O9IACT
PHENOXYETHANOLHIE492ZZ3TIACT
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDEXGN40YQC7BIACT

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
My-Shield Sanitizing BodyBENZALKONIUM CHLORIDEEnviro Specialty Chemicals Incd4ed5da9-cc32-447d-994e-6242c3fb5f782026-01-29WarningsExact identifier
ndc (package): 71884-009-01
ndc (package): 71884-009-05
ndc (package): 71884-009-02
ndc (package): 71884-009-16
ndc (product): 71884-009
ndc11 (package): 71884000916
ndc11 (package): 71884000905
ndc11 (package): 71884000901
ndc11 (package): 71884000902
spl id: c6e7f949-8cc0-4ec5-bc87-9cef5b9aeeec
spl set id: d4ed5da9-cc32-447d-994e-6242c3fb5f78

Reported adverse events (FAERS/openFDA)#

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