KINDEST KARE ADVANCED ANTIMICROBIAL HANDWASH- benzalkonium chloride 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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Kindest Kare® Advanced Antimicrobial Handwash

Drug Facts

Active ingredient

0.7% Benzalkonium Chloride

Purpose

Antiseptic

Use

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

Warnings

For external use only

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

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.

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

Hexylene glycol, Cocamidopropyl amine oxide, PEG-80 Sorbitan laurate, Hydroxypropyl methylcellulose, PEG-150 Distearate, PEG-8 Dimethicone, Sorbitol, Glycerin, Cocamidopropyl PG-Dimonium chloride phosphate, Cocamide MIPA, Soyamidopropyl amine oxide, Lauramine oxide, Phenoxyethanol, Potassium hydroxide, Citric acid

Questions or comments?

800-548-4873

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

Kindest Kare®
Advanced

Antimicrobial
Handwash

NDC 0519-6267-41

Hand Soap

Healthcare Personnel
Handwash

Moisturizing

Fragrance Free

REORDER #
6267-87

1 Liter SDS (33.8 fl oz) (1.05 qt)

STERIS®

STERIS Corporation ◾ 7501 Page Avenue ◾ St. Louis, MO 63133 ◾ USA
800-548-4873 ◾ www.steris.com

62824
6267-86B(F)(417)

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

KINDEST KARE ADVANCED ANTIMICROBIAL HANDWASH
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0519-6267
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0519-6267-87	12 in 1 CASE	11/01/2016	10/26/2018
1	NDC:0519-6267-41	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC:0519-6267-91	18 in 1 CASE	11/01/2016	10/26/2018
2	NDC:0519-6267-13	444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH NOT FINAL	part333E	11/01/2016	10/26/2018

Labeler - STERIS Corporation (139424188)

Revised: 10/2018

Document Id: db1397b3-25bf-4287-8f24-fe6808838d1c

Set id: d10ff7a0-53c1-4c4c-8569-39f5e4fa70cc

Version: 3

Effective Time: 20181030

STERIS Corporation