CLEAN-US PURICHLO SANITIZER-SPRAY- hypochlorous acid liquid

CLEAN-US PURICHLO SANITIZER-Spray by

Drug Labeling and Warnings

CLEAN-US PURICHLO SANITIZER-Spray by is a Otc medication manufactured, distributed, or labeled by KUMWON INTERNATIONAL INC., Multibio Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Hypochlorous Acid 0.005%

Purpose

Sanitizer

Uses

Purpose of sterilizing the surface of instruments and objects.

Warning

This Products are for use on surface, Not humans.

Follow the contact time as directed in the directions.

Do not touch the surface during the contact time.

Do not dilute, use the solution as is.

Stop use and ask a doctor if irritation or redness occurs.

Do not inhale or ingest.

Keep out of reach of children.

Make sure to supervise the use of products by children, the elderly, the disabled, and others who vulnerable to the use of products.

Directions

Spray on the surface of sterilizing object in a wide range.

Spray on a target that requires sterilization and let it dry naturally or wipe with a dry towel after 30 seconds.

If you can’t spray directly on the surface, you can spray to the clean cloth and wipe it off.

Other information

If this product is exposed to external air for a long time it may react with UV or air and be restored to water.

Keep it sealed and store in a cool and dark place.

Inactive ingredients

Water 99.995%

Package Label

INGREDIENTS AND APPEARANCE

CLEAN-US PURICHLO SANITIZER-SPRAY 
hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79543-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.005 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	99.995 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79543-201-01	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/10/2020
2	NDC: 79543-201-02	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/10/2020

Labeler - KUMWON INTERNATIONAL INC. (694803493)

Registrant - Multibio Co., Ltd (693713128)

Establishment
Name	Address	ID/FEI	Business Operations
Multibio Co., Ltd		693713128	manufacture(79543-201)