KINDEST KARE FOAM ANTISEPTIC HANDRUB WITH ENHANCED EMOLLIENTS - alcohol liquid
STERIS Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

62% v/v Ethyl Alcohol

Purpose

Antiseptic

Use

Healthcare Personnel Handwash to decrease transient bacteria on the skin before contact with patients under medical care or treatments.

Warnings

Flammable, keep away from fire or flame.

For external use only. Do not get in the eyes. Eye irritant. If splashed in eyes, rinse promptly and thoroughly with water.

Discontinue use if irritation and redness develop. If irritation persists for more than 3 days, consult a physician.

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Apply product to hands and rub thoroughly until dry.

Inactive ingredients

Deionized water, Bis-PEG-10 Dimethicone/Dimer Dilinoleate, Methylpropanediol, Phenoxyethanol, Behentrimonium Methosulfate, PEG-7 Glyceryl Cocoate, Glycerin, Polyquaternium-6, PEG-45 Palm Kernel Glycerides, Cocamidopropyl PG-Dimonium Chloride Phosphate

Questions or comments?

800-548-4873 www.steris.com

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

NDC 0519-1199-41

KINDEST KARE™ FOAM

Antiseptic Handrub with
Enhanced Emollients

1 Liter SDS (33.8 fl oz) (1.05 qt)
1199-FM

A N T I M I C R O B I A L

No-Rinse Healthcare Personnel Handwash

Mild, Moisturizing Formulation
Fast-acting and Broad-Spectrum
Antimicrobial Efficacy
CHG Compatible
Fragrance and Dye Free

For Hospital and Professional Use

STERIS Corporation ■ 7501 Page Avenue ■ St. Louis, MO 63133 n USA

1199-X3A(F)(911) 62305 SDA-26-20005

Principal Display Panel - 1 Liter Bottle Label

KINDEST KARE FOAM ANTISEPTIC HANDRUB WITH ENHANCED EMOLLIENTS
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0519-1199
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
alcohol (alcohol)	alcohol	62 mg in 100 mL

Inactive Ingredients
Ingredient Name	Strength
water
methylpropanediol
phenoxyethanol
behentrimonium methosulfate
PEG-7 glyceryl cocoate
glycerin

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:0519-1199-41	1000 mL in 1 BOTTLE, PLASTIC	None
2	NDC:0519-1199-13	444 mL in 1 BOTTLE, PLASTIC	None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	11/15/2011

Labeler - STERIS Corporation (139424188)

Establishment
Name	Address	ID/FEI	Operations
STERIS Corporation		139424188	MANUFACTURE

Revised: 10/2011 STERIS Corporation