FDA.reportPublic FDA data

HUUREKA SANITIZER

Manufacturer
KEWS CORPORATION
Effective date
2022-01-18
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:47:10

Label at a glance#

ProductHUUREKA SANITIZER
Active ingredientHYPOCHLOROUS ACID
Label structure14 sections

Dosage and administration

Use when soap and water not available to supplement regular hand washing. Apply liberally to hands and rub hands thoroughly 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 ------ 0.0.007%

Purpose

INDICATIONS & USAGE 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 thoroughly until product is dried.

Spray enough to the suspected tool, furniture and space.

Inactive Ingredient(s)

INACTIVE INGREDIENT SECTION

Water

Intended Use

INTENDED USE OF THE DEVICE

For Personal sanitizing to decrease baceteria on skin

Recommended for repeated use.

Warnings:

WARNINGS SECTION

For External Use

Purpose:

OTC - PURPOSE SECTION

For personal sanitizing to decrease bacteria on skin.

Recommened 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.

100 mL PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100mL NDC 75644-001-001 HUUREKA 100mL PDPHUUREKA 100mL PDP

500 mL PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 mL NDC 75644-001-002 HUUREKA 500mL PDPHUUREKA 500mL PDP

2 LT PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2 LT PDP 75644-001-04

HUUREKA 2LT PDPHUUREKA 2LT PDP

4 LT PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4 LT PDP, NDC: 75644-001-05

Huureka 4LT PDPHuureka 4LT PDP

10 LT PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10 LT PDP, NDC 75644-001-06

Huureka 10L PDPHuureka 10L PDP

20LT PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 LT NDC 75644-001-003 Huureka 20LT PDPHuureka 20LT PDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75644-001-01HUUREKA SANITIZER100 mL in 1 BOTTLE, SPRAYLIQUID1005
75644-001-02HUUREKA SANITIZER500 mL in 1 BOTTLE, SPRAYLIQUID5005
75644-001-03HUUREKA SANITIZER20000 mL in 1 JUGLIQUID200005
75644-001-04HUUREKA SANITIZER2000 mL in 1 JUGLIQUID20005
75644-001-05HUUREKA SANITIZER4000 mL in 1 JUGLIQUID40005
75644-001-06HUUREKA SANITIZER10000 mL in 1 JUGLIQUID100005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75644-001HUUREKA SANITIZER (HYPOCHLOROUS ACID) LIQUID [KEWS CORPORATION]5Legacy NDC, 6 package rows20220119_a3d00ae1-de06-8d54-e053-2995a90a33a4.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
75644-00175644-001-01, 75644-001-02, 75644-001-03, 75644-001-04, 75644-001-05, 75644-001-06

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
HYPOCHLOROUS ACID712K4CDC10ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
d5e06243-b963-7810-e053-2a95a90a7cf5a3d00ae1-de06-8d54-e053-2995a90a33a42022-01-18WarningsExact identifier
spl id: d5e06243-b963-7810-e053-2a95a90a7cf5
spl set id: a3d00ae1-de06-8d54-e053-2995a90a33a4

Reported adverse events (FAERS/openFDA)#

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