KINDEST KARE ANTIMICROBIAL FOAM HANDWASH- triclosan liquid

Kindest Kare Antimicrobial Foam Handwash by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Triclosan 0.75%

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

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

Inactive ingredients

Aqua (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, Parfum (Fragrance)

Questions or comments?

1-866-783-0422

PRINCIPAL DISPLAY PANEL - 444 ml Bottle Label

Kindest Kare®
deb med®

NDC: 11084-808-13

REORDER #
1452-RF

Hand Soap
Antimicrobial Foaming Handwash

15
seconds
Fast-acting

Mild Fragrance

Antimicrobial

Net Contents: 444 ml (15 fl oz)

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

1452-XFESG(F)(917)
61824

INGREDIENTS AND APPEARANCE

KINDEST KARE ANTIMICROBIAL FOAM HANDWASH 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-808
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	7.5 mg  in 1 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: 11084-808-13	444 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2018	02/01/2020
2	NDC: 11084-808-41	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2018	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	02/01/2018	06/01/2020

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
STERIS Corporation		139424188	MANUFACTURE(11084-808)