KLEAN GENIX HAND SANITIZER- alcohol gel

Klean GeniX Hand Sanitizer by

Drug Labeling and Warnings

Klean GeniX Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Custom Chemical Services, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 70% v/v

Purpose

Antibacterial

INDICATIONS & USAGE

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

WARNINGS

Warning Flammable. Keep away from fire or flame. For external use only.

WHEN USING

When using this product avoid contact with eyes, ears, and mouth. In case of contact with eyes, flush eyes with water immediately. Avoid contact with broken skin. Discontinue use if irritation or redness develops. If condition persists, consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. Children should only use this product under adult supervison. Do not drink. Not edible. In case of accidential ingestion, seek professional assistance or contact a Poison Control Center immediately.

STORAGE AND HANDLING

Other Information Store under 105°F. 

DOSAGE & ADMINISTRATION

Directions Place hand sanitizer in your palm, thoroughly cover hands, including between fingers, under fingernails, and around wrists. Rub briskly until dry. No rinsing required.

INACTIVE INGREDIENT

Inactive Ingredients Purified water, Glycerin USP, Carbomer

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KLEAN GENIX HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78174-052
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70.0882 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.0678 L  in 100 L
water (UNII: 059QF0KO0R)	29.4866 L  in 100 L
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)	0.3574   in 100 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78174-052-10	0.004 L in 1 POUCH; Type 0: Not a Combination Product	04/12/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/12/2021

Labeler - Custom Chemical Services, LLC (078305908)

Establishment
Name	Address	ID/FEI	Business Operations
Custom Chemical Services, LLC		078305908	manufacture(78174-052)