CLOH Living Hand Sanitizer

Manufacturer
SpaceLink Corporation
Effective date
2020-07-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:04

Label at a glance#

ProductCLOH Living Hand Sanitizer
Active ingredientHYPOCHLOROUS ACID
Label structure12 sections

Dosage and administration

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.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Hypochlorous Acid 0.0035%. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only-hand.

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLOH Living Hand Sanitizer SprayCLOH Living Hand Sanitizer Spray

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79617-100-01CLOH Living Hand Sanitizer500 mL in 1 BOTTLE, SPRAYSPRAY5001
79617-100-02CLOH Living Hand Sanitizer60 mL in 1 BOTTLE, SPRAYSPRAY601
79617-100-03CLOH Living Hand Sanitizer1000 mL in 1 BOTTLESPRAY10001
79617-100-04CLOH Living Hand Sanitizer4000 mL in 1 BOTTLESPRAY40001
79617-100-05CLOH Living Hand Sanitizer20000 mL in 1 BOTTLESPRAY200001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79617-100CLOH LIVING HAND SANITIZER (HYPOCHLOROUS ACID) SPRAY [SPACELINK CORPORATION]1Legacy NDC, 5 package rows20200721_aae7fef1-0cb3-ba7a-e053-2a95a90ac951.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79617-10079617-100-01, 79617-100-02, 79617-100-03, 79617-100-04, 79617-100-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HYPOCHLOROUS ACID712K4CDC10ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
aae7fd8e-c786-9723-e053-2a95a90a367aaae7fef1-0cb3-ba7a-e053-2a95a90ac9512020-07-20WarningsExact identifier
spl id: aae7fd8e-c786-9723-e053-2a95a90a367a
spl set id: aae7fef1-0cb3-ba7a-e053-2a95a90ac951

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.