KINDEST KARE AIR-INFUSED FOAM ANTISEPTIC HANDRUB- alcohol liquid

Kindest Kare Air-Infused Foam Antiseptic Handrub by

Drug Labeling and Warnings

Kindest Kare Air-Infused Foam Antiseptic Handrub by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc., STERIS Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Uses

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

Warnings

For external use only

Flammable. Keep away from fire or flame.

When using this product do not get it in the eyes; causes eye irritation upon direct contact. In case of eye exposure, rinse thoroughly with water. If eye irritation persists, contact a physician.

Stop use and ask a doctor if irritation and redness develop and persist for more than 3 days.

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

Directions

• Healthcare Personnel Handwash Apply product to hands and rub until thoroughly dry

Inactive ingredients

Aqua (Water), Behentrimonium Methosulfate, Bis-PEG-10 Dimethicone/Dimer Dilinoleate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Diisopropyl Adipate, Glycerin, Methylpropanediol, PEG-6 Caprylic/Capric Glycerides, PEG-7 Glyceryl Cocoate, Phenoxyethanol.

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PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

Kindest Kare
Air-Infused™

NDC: 11084-809-41

deb med®

Hand Sanitizer
Foam Antiseptic Handrub

Excellent
Moisturization

15
seconds
Fast Acting

CHG Compatible

REORDER #
1458-FM

1 Liter (33.8 fl oz) (1.05 qt)

1458-X3C(F)(917)
62570
SDA-26-20005
Product Made in U.S.A.

INGREDIENTS AND APPEARANCE

KINDEST KARE AIR-INFUSED FOAM ANTISEPTIC HANDRUB 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-809
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
Bis-PEG-10 Dimethicone/Dimer Dilinoleate Copolymer (UNII: CF5W1YCX11)
methylpropanediol (UNII: N8F53B3R4R)
phenoxyethanol (UNII: HIE492ZZ3T)
behentrimonium methosulfate (UNII: 5SHP745C61)
PEG-7 glyceryl cocoate (UNII: VNX7251543)
glycerin (UNII: PDC6A3C0OX)
PEG-6 Caprylic/capric glycerides (UNII: GO50W2HWO8)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-809-41	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2018
2	NDC: 11084-809-13	444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/01/2018

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
STERIS Corporation		139424188	MANUFACTURE(11084-809)