BELSON ALCOHOL FREE HAND SANIZITER

Manufacturer
KEWS CORPORATION
Effective date
2022-01-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:10

Label at a glance#

ProductBELSON ALCOHOL FREE HAND SANIZITER
Active ingredientHYPOCHLOROUS ACID
Label structure13 sections

Indications and uses

-For personal sanitzing to decrease bacteria on skin -Recommended for repeated use

Dosage and administration

-Use when soap and water not available to supplement regular hand washing. -Apply liberally to hands and rub hands thorougly until product is dried -Spray enough to the suspected tool, furniture and space.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

HYPOCHLOROUS ACID -- 0.007%

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Directions for Use

DOSAGE & ADMINISTRATION SECTION

-Use when soap and water not available to supplement regular hand washing.

-Apply liberally to hands and rub hands thorougly until product is dried

-Spray enough to the suspected tool, furniture and space.

Intended Use

INDICATIONS & USAGE SECTION

-For personal sanitizing to decrease bacteria on skin

-Recommended for repeated use

USES

OTC - PURPOSE SECTION

-For personal sanitzing to decrease bacteria on skin

-Recommended for repeated use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

WARNINGS SECTION

For External Use

100mL PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BELSON 100mL PDPBELSON 100mL PDP100mL NDC 75644-003-01

500mL PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BELSON 500ML PDPBELSON 500ML PDP500mL NDC 75644-003-02

1LT PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1LT NDC 75644-003-03 BELSON 1LT PDPBELSON 1LT PDP

4LT PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4LT NDC 75644-003-04 BELSON 4L PDPBELSON 4L PDP

20LT PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BELSON 20LT PDPBELSON 20LT PDP20LT NDC 75644-003-05

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75644-003-01BELSON ALCOHOL FREE HAND SANIZITER100 mL in 1 BOTTLE, SPRAYLIQUID1002
75644-003-02BELSON ALCOHOL FREE HAND SANIZITER500 mL in 1 BOTTLE, SPRAYLIQUID5002
75644-003-03BELSON ALCOHOL FREE HAND SANIZITER1000 mL in 1 JUGLIQUID10002
75644-003-04BELSON ALCOHOL FREE HAND SANIZITER4000 mL in 1 JUGLIQUID40002
75644-003-05BELSON ALCOHOL FREE HAND SANIZITER20000 mL in 1 JUGLIQUID200002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75644-003BELSON ALCOHOL FREE HAND SANIZITER (HYPOCHLOROUS ACID) LIQUID [KEWS CORPORATION]2Legacy NDC, 5 package rows20220119_a878ee09-6689-e374-e053-2995a90a7aad.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75644-00375644-003-01, 75644-003-02, 75644-003-03, 75644-003-04, 75644-003-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HYPOCHLOROUS ACID712K4CDC10ACTIB

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
d5e073ac-61a8-226a-e053-2a95a90a3db0a878ee09-6689-e374-e053-2995a90a7aad2022-01-18WarningsExact identifier
spl id: d5e073ac-61a8-226a-e053-2a95a90a3db0
spl set id: a878ee09-6689-e374-e053-2995a90a7aad

Reported adverse events (FAERS/openFDA)#

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