KINDEST KARE ADVANCED ANTIMICROBIAL HANDWASH- benzalkonium chloride liquid

Kindest Kare Advanced Antimicrobial Handwash by

Drug Labeling and Warnings

Kindest Kare Advanced Antimicrobial 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 0.7%

Purpose

Antiseptic

Uses

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

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, Cocamidopropylamine Oxide, PEG- 80 Sorbitan Laurate, Hydroxypropyl Methylcellulose, PEG-150 Distearate, PEG-8 Dimethicone, Sorbitol, Glycerin, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocamide MIPA, Soyamidopropylamine Oxide, Lauramine Oxide, Phenoxyethanol, Potassium Hydroxide, Citric Acid

Questions or comments?

1-866-783-0422

PRINCIPAL DISPLAY PANEL - 444 mL Bottle Label

Kindest Kare®
Advanced

deb med®

NDC: 11084-806-13

REORDER #
6267-R2

Hand Soap
Antimicrobial 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

6267-14B(F)(318)
62826

INGREDIENTS AND APPEARANCE

KINDEST KARE ADVANCED ANTIMICROBIAL HANDWASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-806
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.7 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
PEG-80 SORBITAN LAURATE (UNII: 239B50Y732)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-806-41	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/01/2018
2	NDC: 11084-806-13	444 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(11084-806)