HYPOCHLOROUS ACID HAND SANITIZER- hypochlorous acid liquid

Hypochlorous Acid Hand Sanitizer by

Drug Labeling and Warnings

Hypochlorous Acid Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Shenzhen Risai Medical Technology Co., Ltd, A03 Lab of BTS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hypochlorous acid 100 mg/L. Purpose: Sanitation.

Purpose

Kill germs and viruses, keep hands sanitated, protect health from disease or pandmics.

Use

Hand disinfection for medical staff, or hand sanitation of families, enterprise or public places. It's suitable as well for hand sanitation of children, women and aged people.

Warnings

For external use only.

Do not use for eyes disinfection.

Keep out of reach of children.

Do not use

Do not use for eyes disinfection.

Cautions

The product is normally not irritation to human skin or mucosa. If you feel uncomfortable in case of contact of eyes, please rinse or clean it with water. If swallowed and fee unwell, please get medical help.

Stop use

If you feel uncomfortable in case of contact of eyes, please rinse or clean it with water. If swallowed and fee unwell, please get medical help.

Keep out of reach of children

Keep out of reach of children.

Method to use

Press the nozzle to soak the hand, keep rubbing hands for 1 minute.

Storage

Keep away from heat and sunlight.

Store in room temperature and in cool place.

Inactive ingredient

Water

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HYPOCHLOROUS ACID HAND SANITIZER 
hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81934-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	50 mg  in 500 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81934-101-05	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/25/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/25/2021

Labeler - Shenzhen Risai Medical Technology Co., Ltd (710909218)

Registrant - A03 Lab of BTS (548009541)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Risai Medical Technology Co., Ltd		710909218	manufacture(81934-101) , label(81934-101)