KINDEST KARE AIR-INFUSED FOAM ANTISEPTIC HANDRUB- alcohol liquid 
SC Johnson Professional 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 Air-Infused™ Foam Antiseptic Handrub

Drug Facts

Active ingredient

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Uses

Warnings

For external use only

Flammable. Keep away from fire or flame.

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

Inactive ingredients

Aqua (Water), Behentrimonium Methosulfate, Bis-PEG-10 Dimethicone/Dimer Dilinoleate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Diisopropyl Adipate, Glycerin, Methylpropanediol, PEG-6 Caprylic/Capric Glycerides, PEG-7 Glyceryl Cocoate, Phenoxyethanol.

Questions or comments?

1-866-783-0422

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

SCJ PROFESSIONAL
HEALTHCARE

Kindest Kare Air Infused™

NDC 11084-809-41

Hand Sanitizer
Foamed Antiseptic Handrub

Excellent
Moisturization

15
seconds
Fast
Acting

CHG
Compatible

1 Liter (33.8 fl oz) (1.05 qt)
SAP # 4000000041

REORDER #
1458-FM

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

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SKIN CARE

Principal Display Panel - 1 Liter Bottle Label
KINDEST KARE AIR-INFUSED FOAM ANTISEPTIC HANDRUB 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-809
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
Bis-PEG-10 Dimethicone/Dimer Dilinoleate Copolymer (UNII: CF5W1YCX11)  
methylpropanediol (UNII: N8F53B3R4R)  
phenoxyethanol (UNII: HIE492ZZ3T)  
behentrimonium methosulfate (UNII: 5SHP745C61)  
PEG-7 glyceryl cocoate (UNII: VNX7251543)  
glycerin (UNII: PDC6A3C0OX)  
CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6 (UNII: GO50W2HWO8)  
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-809-411000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/01/2018
2NDC:11084-809-13444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/01/201804/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/01/2018
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
STERIS Corporation139424188MANUFACTURE(11084-809)

Revised: 12/2020
Document Id: 471e5a1d-fcd1-4920-a609-63d7d599c519
Set id: 6483aaa7-51db-404a-8c18-f96173f5c40b
Version: 2
Effective Time: 20201221
 
SC Johnson Professional USA, Inc.