BELSON ALCOHOL FREE HAND SANIZITER- hypochlorous acid liquid

BELSON ALCOHOL FREE HAND SANIZITER by

Drug Labeling and Warnings

BELSON ALCOHOL FREE HAND SANIZITER by is a Otc medication manufactured, distributed, or labeled by KEWS CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

100mL NDC: 75644-003-01

500mL PDP

500mL NDC: 75644-003-02

1LT PDP

1LT NDC: 75644-003-03

4LT PDP

4LT NDC: 75644-003-04

20LT PDP

20LT NDC: 75644-003-05

INGREDIENTS AND APPEARANCE

BELSON ALCOHOL FREE HAND SANIZITER 
hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75644-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.007 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75644-003-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/19/2020
2	NDC: 75644-003-02	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/19/2020
3	NDC: 75644-003-03	1000 mL in 1 JUG; Type 0: Not a Combination Product	06/19/2020
4	NDC: 75644-003-04	4000 mL in 1 JUG; Type 0: Not a Combination Product	06/19/2020
5	NDC: 75644-003-05	20000 mL in 1 JUG; Type 0: Not a Combination Product	06/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/19/2020

Labeler - KEWS CORPORATION (688640317)

Registrant - KEWS CORPORATION (688640317)

Establishment
Name	Address	ID/FEI	Business Operations
KEWS CORPORATION		688640317	manufacture(75644-003) , pack(75644-003) , label(75644-003)