STERiZAR

Manufacturer
Unicorn Media Partners LLC
Effective date
2021-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:36:57

Label at a glance#

ProductSTERiZAR Advanced Barrier Control
Active ingredientBenzalkonium Chloride
Label structure10 sections

Dosage and administration

Apply a small amount of product to the hands and rub in well, paying particular attention to fingernails and the area between the fingers. Allow hands to air dry. Important- the use of towels or tissue may lead to recontamination with bacteria.

Storage and handling

Store in cool dry area. Avoid freezing Store at 15-30 C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 1.6 %

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Sanitizing Hand Wash for Hand Washing to Decrease Bacteria on Skin. For Repeated Use.

Warnings

WARNINGS SECTION

For external use only. Keep away from heat. Flammable, Keep Away from Heat and Flame

Do not use

OTC - DO NOT USE SECTION

  • On open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rush occurs These may be sign of serious medical conditions.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away at 1-800-222-1222

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a small amount of product to the hands and rub in well, paying particular attention to fingernails and the area between the fingers.
  • Allow hands to air dry.
  • Important- the use of towels or tissue may lead to recontamination with bacteria.

Other information

STORAGE AND HANDLING SECTION

  • Store in cool dry area.
  • Avoid freezing
  • Store at 15-30 C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Amines, Blue Dye,C12-14 Alkyl dimethyl, Decyl Dimethyl Ammonium Chloride, Fragrance, N-oxides, Purified Water, Sodium Ethyl Hexyl Sulfate.

SPL UNCLASSIFIED SECTION

Imported and distributed by
Unicorn Media Partners LLC
41 E. Sunrise Hwy.
Lindenhurst, NY 11757

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 79310-302-22

STERiZAR®
Advanced Barrier Control

Antibacterial
Sanitizing
Hand Wash

Specially formulated to kill
harmful bacteria

ALCOHOL
FREE
Kills 99.999% of germs

2 Hours
Protection after Rinsing

16.9 FL OZ (500 mL)

• HALAL MONITORING •
COMMITTEE - UK

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2462801benzalkonium chloride 1.6 % Medicated Liquid SoapPSN2
2462801benzalkonium chloride 16 MG/ML Medicated Liquid SoapSCD2
2462801benzalkonium chloride 1.6 % Medicated Liquid SoapSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79310-302-21STERiZAR Advanced Barrier Control5000 mL in 1 BOTTLE, PLASTICSOAP50002
79310-302-22STERiZAR Advanced Barrier Control500 mL in 1 BOTTLE, PUMPSOAP5002
79310-302-27STERiZAR Advanced Barrier Control285 mL in 1 BOTTLE, PLASTICSOAP2852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79310-302STERIZAR ADVANCED BARRIER CONTROL (BENZALKONIUM CHLORIDE) SOAP [UNICORN MEDIA PARTNERS LLC]2Legacy NDC, 3 package rows20210115_4f39dc81-485a-4639-a12a-67b3225d77d0.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79310-30279310-302-22, 79310-302-21, 79310-302-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a8eac16a-6eea-481e-930f-ece9458da2a34f39dc81-485a-4639-a12a-67b3225d77d02021-01-14WarningsExact identifier
spl id: a8eac16a-6eea-481e-930f-ece9458da2a3
spl set id: 4f39dc81-485a-4639-a12a-67b3225d77d0

Reported adverse events (FAERS/openFDA)#

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