OTC Medication Information: CLOH Living Hand Sanitizer

CLOH LIVING HAND SANITIZER- hypochlorous acid spray
SpaceLink Corporation

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.

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
(click image for full-size original)

CLOH LIVING HAND SANITIZER
hypochlorous acid spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:79617-200
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYPOCHLOROUS ACID (HYPOCHLOROUS ACID) HYPOCHLOROUS ACID 0.0035 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
Product Characteristics
Color Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:79617-200-01 500 mL in 1 BOTTLE, SPRAY None
2 NDC:79617-200-02 60 mL in 1 BOTTLE, SPRAY None
3 NDC:79617-200-03 1000 mL in 1 BOTTLE None
4 NDC:79617-200-04 4000 mL in 1 BOTTLE None
5 NDC:79617-200-05 20000 mL in 1 BOTTLE None
Image of Product
(click image for full-size original)
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 Operations
SpaceLink Corporation 695898222 manufacture (79617-200)

Revised: 06/2022 SpaceLink Corporation

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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