BELSON ALCOHOL FREE HAND SANIZITER- 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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BELSON ALCOHOL FREE HAND SANITIZER

ACTIVE INGREDIENT

HYPOCHLOROUS ACID -- 0.007%

Inactive Ingredients

Water

Purpose

Antimicrobial

Directions for Use

-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

-For personal sanitizing to decrease bacteria on skin

-Recommended for repeated use

USES

-For personal sanitzing to decrease bacteria on skin

-Recommended for repeated use

Keep out of reach of children.

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

Warnings

For External Use

100mL PDP

BELSON 100mL PDP100mL NDC 75644-003-01

500mL PDP

BELSON 500ML PDP500mL NDC 75644-003-02

1LT PDP

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

4LT PDP

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

20LT PDP

BELSON 20LT PDP20LT NDC 75644-003-05

BELSON ALCOHOL FREE HAND SANIZITER 
hypochlorous acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75644-003
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:75644-003-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/19/2020
2NDC:75644-003-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/19/2020
3NDC:75644-003-031000 mL in 1 JUG; Type 0: Not a Combination Product06/19/2020
4NDC:75644-003-044000 mL in 1 JUG; Type 0: Not a Combination Product06/19/2020
5NDC:75644-003-0520000 mL in 1 JUG; Type 0: Not a Combination Product06/19/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/19/2020
Labeler - KEWS CORPORATION (688640317)
Registrant - KEWS CORPORATION (688640317)
Establishment
NameAddressID/FEIBusiness Operations
KEWS CORPORATION688640317manufacture(75644-003) , pack(75644-003) , label(75644-003)

Revised: 1/2022
Document Id: d5e073ac-61a8-226a-e053-2a95a90a3db0
Set id: a878ee09-6689-e374-e053-2995a90a7aad
Version: 2
Effective Time: 20220118
 
KEWS CORPORATION