KINDEST KARE HAND ANTIMICROBIAL HANDWASH- chloroxylenol soap

Kindest Kare Hand by

Drug Labeling and Warnings

Kindest Kare Hand by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc., APEX International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Chloroxylenol 1.0%

Purpose

Antiseptic

Uses

• Antiseptic 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; this product 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 symptoms persist for more than 3 days.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet skin and spread a small amount on the hands
• wash hands, rinse thoroughly with water, and repeat as necessary between patient contacts

Inactive ingredients

aqua (water), propylene glycol, sodium lauroyl sarcosinate, PEG-150 distearate, disodium cocoamphodiacetate, polyquaternium-7, tetrasodium EDTA acrylates/PEG-10 maleate/styrene copolymer, citric acid, parfum (fragrance).

Questions or comments?

1-866-783-0422

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

SCJ PROFESSIONAL
HEALTHCARE

Kindest Kare®

NDC: 11084-036-41

Hand Soap
Antimicrobial Handwash

Acute Kare

Antimicrobial
Moisturising
Mild Fragrance

Manufactured for:
SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-866-783-0422
www.scjp.com

REORDER #
1206-87

1 Liter SDS (33.8 fl oz)

4000009725

DCN9362 / 0221

deb
SKIN CARE

INGREDIENTS AND APPEARANCE

KINDEST KARE HAND   ANTIMICROBIAL HANDWASH
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
EDETATE SODIUM (UNII: MP1J8420LU)
METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-036-41	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2022	12/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	505G(a)(3)	02/01/2022	12/31/2026

Labeler - SC Johnson Professional USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
APEX International, Inc.		015226132	MANUFACTURE(11084-036)