Active Ingredient(s)

Hypochlorous Acid 0.0035%. Purpose: Antimicrobial

Purpose

Antimicrobial, Hand Sanitizer

Use

Hand sanitizer to help reduce bacteria on the skin.
Recommended for repeated use.

Warnings

For external use only-hand.

Do not use

in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.
For children under 6, use only under adult supervision.
Not recommended for infants.

Other information

Store at room temperature 1oC-30oC ( 33.8oF-86oF).

Inactive ingredients

Purified Water.

Package Label - Principal Display Panel

CLOH Living Hand Sanitizer Spray

CLOH LIVING HAND SANITIZER
hypochlorous acid spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79617-200
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.0035 g in 100 mL

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

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:79617-200-01	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2022
2	NDC:79617-200-02	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/17/2022
3	NDC:79617-200-03	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2022
4	NDC:79617-200-04	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2022
5	NDC:79617-200-05	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		06/17/2022

Labeler - SpaceLink Corporation (689464352)

Registrant - SpaceLink Corporation (695898222)

Name	Address	ID/FEI	Business Operations
Establishment
SpaceLink Corporation		695898222	manufacture(79617-200)