KLEANERLAB HAND SANITIZER- alcohol gel

Kleanerlab Hand Sanitizer by

Drug Labeling and Warnings

Kleanerlab Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Laboratorios Elizondo S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

• To decrease bacteria on the skin that could cause disease
• Recommended for repeated use.

Warnings

For external use only: hands.

Flammable, keep away from fire or flame.

When using this product

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest. If skin irritation occurs seek medical advice.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place a small amount of gel in your palm and rub hands together until dry.
• For children under 6, use only under adult supervision.
• Not recommended for infants

Other information

• Do not store above 110°F.
• May discolor some fabrics.
• Harmful to wood finishes and plastics.

Inactive ingredients

Water, USP Glycerin, Carbopol 940, Triethanolamine.

Questions or comments?

www.kleanerlab.com

Package Labeling:250 mL

Package Labeling:1 L

INGREDIENTS AND APPEARANCE

KLEANERLAB HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80226-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80226-000-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/23/2020
2	NDC: 80226-000-02	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/23/2020

Labeler - Laboratorios Elizondo S.A. de C.V. (951582747)