HUUREKA SANITIZER- hypochlorous acid liquid 
KEWS CORPORATION

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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HUUREKA SANITIZER

Active Ingredient

Hypochlorous Acid ------ 0.0.007%

Purpose

Antimicrobial

Directions for Use:

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)

Water

Intended Use

For Personal sanitizing to decrease baceteria on skin

Recommended for repeated use.

Warnings:

For External Use

Purpose:

For personal sanitizing to decrease bacteria on skin.

Recommened for repeated use.

Keep out of reach of children.

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

100 mL PDP

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

500 mL PDP

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

2 LT PDP

2 LT PDP 75644-001-04

HUUREKA 2LT PDP

4 LT PDP

4 LT PDP, NDC: 75644-001-05

Huureka 4LT PDP

10 LT PDP

10 LT PDP, NDC 75644-001-06

Huureka 10L PDP

20LT PDP

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

HUUREKA SANITIZER 
hypochlorous acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75644-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.007 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75644-001-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2020
2NDC:75644-001-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2020
3NDC:75644-001-0320000 mL in 1 JUG; Type 0: Not a Combination Product05/01/2020
4NDC:75644-001-042000 mL in 1 JUG; Type 0: Not a Combination Product08/05/2020
5NDC:75644-001-054000 mL in 1 JUG; Type 0: Not a Combination Product08/05/2020
6NDC:75644-001-0610000 mL in 1 JUG; Type 0: Not a Combination Product08/05/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/01/2020
Labeler - KEWS CORPORATION (688640317)
Registrant - KEWS CORPORATION (688640317)
Establishment
NameAddressID/FEIBusiness Operations
KEWS CORPORATION688640317pack(75644-001) , manufacture(75644-001) , label(75644-001)

Revised: 1/2022
Document Id: d5e06243-b963-7810-e053-2a95a90a7cf5
Set id: a3d00ae1-de06-8d54-e053-2995a90a33a4
Version: 5
Effective Time: 20220118
 
KEWS CORPORATION