CLEAN-US PURICHLO SANITIZER-SPRAY- hypochlorous acid liquid 
KUMWON INTERNATIONAL INC.

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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79543-201

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

79543-201-01 60ml Label

79543-201-02 500ml Label

CLEAN-US PURICHLO SANITIZER-SPRAY 
hypochlorous acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79543-201
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.005 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 99.995 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79543-201-0160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/10/2020
2NDC:79543-201-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/21/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/10/2020
Labeler - KUMWON INTERNATIONAL INC. (694803493)
Registrant - Multibio Co., Ltd (693713128)
Establishment
NameAddressID/FEIBusiness Operations
Multibio Co., Ltd693713128manufacture(79543-201)

Revised: 9/2020
Document Id: afe0bfc2-0823-13c4-e053-2995a90a1319
Set id: aa0f2def-f6bf-4d5d-e053-2995a90a9cd5
Version: 3
Effective Time: 20200922
 
KUMWON INTERNATIONAL INC.