KINDEST KARE ADVANCED ANTIMICROBIAL FOAM HANDWASH- benzalkonium chloride liquid

Kindest Kare Advanced Antimicrobial Foam Handwash by

Drug Labeling and Warnings

Kindest Kare Advanced Antimicrobial Foam Handwash 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

Benzalkonium Chloride 0.50%

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

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

Wet hands and apply a small amount of product. Wash hands, rinse thoroughly with water, and repeat as necessary between patient contacts.

Inactive ingredients

Aqua (Water), Hexylene Glycol, Glycerin, PEG-8 Dimethicone, PEG-150 Distearate, Sorbitol, Decyl Glucoside, Soyamidopropyl Amine Oxide, Cocamide MIPA, Cetyl Hydroxyethylcellulose, Polyquaternium-7, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocamidopropyl Amine Oxide, Lauramine Oxide, Citric Acid, Potassium Hydroxide, Phenoxyethanol.

Questions or comments?

1-866-783-0422

PRINCIPAL DISPLAY PANEL - 444 mL Bottle Label

Kindest Kare®
Advanced

deb med®

NDC: 11084-807-13

REORDER #
6264-FH

Hand Soap
Antimicrobial Foaming Handwash

Healthcare Personnel
Handwash

Moisturizing

Fragrance Free

Net Contents: 444 mL (15 fl oz)

Manufactured for:
Deb USA, Inc., Charlotte, NC 28217
1-866-783-0422
www.debmed.com

6264-XFB(F)(917)
62767

INGREDIENTS AND APPEARANCE

KINDEST KARE ADVANCED ANTIMICROBIAL FOAM HANDWASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-807
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
SORBITOL (UNII: 506T60A25R)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-807-41	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2018
2	NDC: 11084-807-13	444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2018
3	NDC: 11084-807-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/01/2018
4	NDC: 11084-807-12	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/01/2018

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(11084-807)