CLOH LIVING HAND SANITIZER- hypochlorous acid spray

CLOH Living Hand Sanitizer by

Drug Labeling and Warnings

CLOH Living Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SpaceLink Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

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

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

INGREDIENTS AND APPEARANCE

CLOH LIVING HAND SANITIZER 
hypochlorous acid spray

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

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

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

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
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 Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/17/2022

Labeler - SpaceLink Corporation (689464352)

Registrant - SpaceLink Corporation (695898222)

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