KLENSKIN HAND SANITIZER- ethyl alcohol gel

KLENSKIN HAND SANITIZER by

Drug Labeling and Warnings

KLENSKIN HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by CoLabs Intl. Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

ETHYL ALCOHOL 70% W/W

PURPOSE

ANTISEPTIC

USES

• Decreases bacteria on hands (skin)
• Recommended for repeated use

WARNINGS

Flammable Keep away from flame, spark, or temperatures above 40°C (104°F)

For external use only.

Do not use on damaged or broken skin.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WHEN USING

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water immediately. If product is
swallowed, get medical help or contact Poison Control Center right away. Stop Use and ask Doctor if rash or irritation develops.

DIRECTIONS

Apply on dry hand and rub into skin until dry. No rinsing required. Repeat as needed.

INACTIVE INGREDIENTS

Water, Glycerin, Thymol, Citrus Aurantium Dulcis (Orange) Peel Oil, Polyacrylate Crosspolymer-6

QUESTIONS OR COMMENTS?

PLEASE CALL TOLL FREE 888.878.5536

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KLENSKIN HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61369-402
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
THYMOL (UNII: 3J50XA376E)
ORANGE OIL (UNII: AKN3KSD11B)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61369-402-64	1892 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/06/2020
2	NDC: 61369-402-29	85 mL in 1 POUCH; Type 0: Not a Combination Product	11/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/06/2020

Labeler - CoLabs Intl. Corp (829850879)