KINDEST KARE ANTIMICROBIAL FOAMING HANDWASH HEALTHCARE PERSONNEL HANDWASH- triclosan liquid

Kindest Kare Antimicrobial Foaming Handwash by

Drug Labeling and Warnings

Kindest Kare Antimicrobial Foaming Handwash by is a Otc medication manufactured, distributed, or labeled by STERIS Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

0.75% Triclosan

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

Apply a small amount to hands. Wash hands, rinse thoroughly with water, and repeat as necessary between patient contacts.

Inactive ingredients

Water, Hexylene glycol, Propyl alcohol, Propylene glycol, Sorbitol, PEG-150 distearate, Sodium lauroyl methyl isethionate, PEG-45 palm kernel glycerides, PEG-7 glyceryl cocoate, C12-C15 alkyl benzoate, Ethanolamine lauroyl sarcosinate, Cocamide MEA, Diammonium EDTA, Citric acid, Ammonium lauryl sulfate, Ethanolamine, Fragrance

Questions or comments?

800-548-4873

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

Kindest Kare®

Antimicrobial
Foaming Handwash

NDC: 0519-1452-41

Hand Soap

15
seconds
Fast-acting

Mild Fragrance

Antimicrobial

REORDER #
1452-FM

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

STERIS®

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

1452-X7D(F)(1014)

62453

INGREDIENTS AND APPEARANCE

KINDEST KARE ANTIMICROBIAL FOAMING HANDWASH   HEALTHCARE PERSONNEL HANDWASH
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0519-1452
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	0.75 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
Hexylene glycol (UNII: KEH0A3F75J)
Propyl alcohol (UNII: 96F264O9SV)
Propylene glycol (UNII: 6DC9Q167V3)
Sorbitol (UNII: 506T60A25R)
PEG-150 distearate (UNII: 6F36Q0I0AC)
sodium lauroyl methyl isethionate (UNII: II6VCD3S6R)
Peg-45 Palm Kernel Glycerides (UNII: UC117W498W)
PEG-7 glyceryl cocoate (UNII: VNX7251543)
Alkyl (C12-15) benzoate (UNII: A9EJ3J61HQ)
Lauroyl sarcosine (UNII: LIJ19P3L6F)
Coco monoethanolamide (UNII: C80684146D)
Edetic Acid (UNII: 9G34HU7RV0)
Citric acid monohydrate (UNII: 2968PHW8QP)
Ammonium lauryl sulfate (UNII: Q7AO2R1M0B)
Monoethanolamine (UNII: 5KV86114PT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0519-1452-91	18 in 1 CASE
1	NDC: 0519-1452-13	444 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 0519-1452-92	6 in 1 CASE
2	NDC: 0519-1452-41	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 0519-1452-87	12 in 1 CASE
3	NDC: 0519-1452-41	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	03/14/2006

Labeler - STERIS Corporation (139424188)

Establishment
Name	Address	ID/FEI	Business Operations
STERIS Corporation		139424188	MANUFACTURE(0519-1452)