ElimiShield Home and Outdoor Moisturizing Hand Sanitizer

Manufacturer
Bryson Industries Inc.
Effective date
2023-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:59:44

Label at a glance#

ProductElimiShield Home and Outdoor Moisturizing Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

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

Dosage and administration

Apply a small amount into palms of hands and spread throughout body. Rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic Skin Sanitizer

Uses

INDICATIONS & USAGE SECTION

  • Sanitizer to help decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Do not use 

OTC - DO NOT USE SECTION

  • in ears or mouth and avoid mucus membranes.

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 a small amount into palms of hands and spread throughout body.
  • Rub into skin until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Polyaminopropyl biguanide, 1-Octadecanaminium NN Dimethyl (3-Trimethoxysilyl) Propyl Chloride, Glycerin, Aloe Barbadenis Leaf Juice Extract, Caprylyl Glucoside, Citric Acid, DL Citronellol, Laureth-4, Phenoxyethanol.

Package Labeling:50ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:200ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN2
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD2
1049254benzalkonium chloride 0.13 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71853-006-01ElimiShield Home and Outdoor Moisturizing Hand Sanitizer50 mL in 1 BOTTLELIQUID502
71853-006-02ElimiShield Home and Outdoor Moisturizing Hand Sanitizer200 mL in 1 BOTTLELIQUID2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71853-006ELIMISHIELD HOME AND OUTDOOR MOISTURIZING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [BRYSON INDUSTRIES INC.]2Current NDC, Legacy NDC, 2 package rows20231110_affeb47c-0e10-7f04-e053-2a95a90a4f1f.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71853-00671853-006-01, 71853-006-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
ElimiShield Home and Outdoor Moisturizing Hand SanitizerBENZALKONIUM CHLORIDEBryson Industries Inc.affeb47c-0e10-7f04-e053-2a95a90a4f1f2023-11-09WarningsExact identifier
ndc (package): 71853-006-02
ndc (package): 71853-006-01
ndc (product): 71853-006
ndc11 (package): 71853000601
ndc11 (package): 71853000602
spl id: 09c2d98f-43b9-301f-e063-6394a90aff3f
spl set id: affeb47c-0e10-7f04-e053-2a95a90a4f1f

Reported adverse events (FAERS/openFDA)#

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