KINDEST KARE ANTIMICROBIAL FOAM HANDWASH- triclosan liquid 
Deb USA, Inc.

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® Antimicrobial Foam Handwash

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

PRINCIPAL DISPLAY PANEL - 444 ml Bottle Label
KINDEST KARE ANTIMICROBIAL FOAM HANDWASH 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-808
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN7.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-808-13444 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/201802/01/2020
2NDC:11084-808-411000 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/201806/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E02/01/201806/01/2020
Labeler - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
STERIS Corporation139424188MANUFACTURE(11084-808)

Revised: 7/2019
Document Id: b3de10ea-d0aa-4589-9720-3103aea33c55
Set id: d0cf5836-ddba-4701-bde8-83e50490b015
Version: 3
Effective Time: 20190702
 
Deb USA, Inc.