FDA.reportPublic FDA data

TRIPLE SHIELD SANITIZING HAND WIPES

Manufacturer
Enviro Specialty Chemicals Inc
Effective date
2021-12-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:45:35

Label at a glance#

ProductTRIPLE SHIELD SANITIZING HAND WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

Sanitizing Hand Wipes to help decrease bacteria on the skin. Recommended for single use. 

Dosage and administration

Wipe liberally over the hands & body, rub into skin until dry. Recommended for single use.

Label contents#

Full prescribing information#

DIRECTIONS FOR USE:

DOSAGE & ADMINISTRATION SECTION

Wipe liberally over the hands & body, rub into skin until dry. Recommended for single use.

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PURPOSE:

OTC - PURPOSE SECTION

Antiseptic/Hand & Skin Sanitizer

USES:

INDICATIONS & USAGE SECTION

Sanitizing Hand Wipes to help decrease bacteria on the skin. Recommended for single use. 

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Laureth-4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl steardimonium

Chloride.

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.

• Children should be supervised when using this product.

QUESTIONS?

OTC - QUESTIONS SECTION

+1(888) 397-8731

SPL UNCLASSIFIED SECTION

WITH SOOTHING ALOE VERA

LONG-LASTING, ALCOHOL-FREE PROTECTION FROM GERMS

Formulated and enhanced with

Zetrisil®

A PROPRIETARY SILICONE QUATERNARY SOLUTION

KILLS 99.99% OF HARMFUL GERMS IN 15 SECONDS!

FAST ACTING 15 SECOND FORMULA

SEE BACK PANEL FOR PRECAUTIONARY STATEMENTS AND FIRST AID

100% LINT FREE

BLEACH FREE

Please dispose of used wipes responsibly.

Do not dispose used wipes down the toilet.

DISTRIBUTED BY TRIPLEROOT®

10004 WURZBACH RD. #104

SAN ANTONIO, TX 78230

www.tripleshieldusa.com

sales@tripleroot.com

FORMULATED IN THE USA | MADE IN CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

PackagingPackaging

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN2
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD2
1038558benzalkonium chloride 0.13 % Topical ClothSY2
1038558benzalkonium chloride 0.13 % Topical SwabSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY2
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71884-030-202024-01-30C16284748780-11030e365-310c-111a-e063-dadaa90a10e2TRIPLE SHIELD SANITIZING HAND WIPES
71884-030-802024-01-30C16284748780-11030e365-310c-111a-e063-dadaa90a10e2TRIPLE SHIELD SANITIZING HAND WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71884-030-20TRIPLE SHIELD SANITIZING HAND WIPES5.25 mL in 1 PATCHCLOTH5.252
71884-030-20TRIPLE SHIELD SANITIZING HAND WIPES20 in 1 PACKETCLOTH202
71884-030-80TRIPLE SHIELD SANITIZING HAND WIPES5.25 mL in 1 PATCHCLOTH5.252
71884-030-80TRIPLE SHIELD SANITIZING HAND WIPES80 in 1 CONTAINERCLOTH802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71884-030TRIPLE SHIELD SANITIZING HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [ENVIRO SPECIALTY CHEMICALS INC]2Legacy NDC, 4 package rows20211212_b1326fad-4160-4920-b2a5-fa838d3ec898.zip

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
71884-03071884-030-20, 71884-030-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CAPRYLYL GLUCOSIDEV109WUT6RLIACT
LAURETH-46HQ855798JIACT
POLIHEXANIDE322U039GMFIACT
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
2189a53b-eb2f-4147-9e56-90e8196c3118b1326fad-4160-4920-b2a5-fa838d3ec8982021-12-09WarningsExact identifier
spl id: 2189a53b-eb2f-4147-9e56-90e8196c3118
spl set id: b1326fad-4160-4920-b2a5-fa838d3ec898

Reported adverse events (FAERS/openFDA)#

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