ALCARE OR FOAMED ANTISEPTIC HANDRUB- alcohol aerosol, foam 
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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Alcare OR® Foamed 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

  • avoid contact with eyes. If splashed in eyes, rinse promptly and thoroughly with water.
  • do not puncture or incinerate; contents under pressure.

Stop use and ask a doctor if

  • irritation and redness develop. If irritation persists for more than 3 days, consult a physician.

Keep out of reach of children

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Other information

Do not store above 120°F (49°C).

For best foam density store and use at 55 - 85°F (13 - 29°C).

Inactive ingredients

Aqua (Water), Hydrofluorocarbon 152A, Isobutane, Emulsifying Wax, Polyquaternium-6, Sodium Benzoate, Propane, Sodium Sesquicarbonate

Questions or comments?

1-866-783-0422

PRINCIPAL DISPLAY PANEL - 482 g Can Label

SCJ PROFESSIONAL
HEALTHCARE

Alcare OR®

NDC 11084-802-80

Hand Sanitizer
Foamed Antiseptic Handrub

Excellent
Moisturization

Surgical Scrub

CHG Compatible

Net Weight: 482 g (17 oz)
SAP # 4000000090

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

REORDER #
6396-80

deb
SKIN CARE

6396-71H(817)

Principal Display Panel - 482 g Can Label
ALCARE OR FOAMED ANTISEPTIC HANDRUB 
alcohol aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-802
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
ISOBUTANE (UNII: BXR49TP611)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
POLYQUATERNIUM-6 (15000 MW) (UNII: YFL33X52PX)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
PROPANE (UNII: T75W9911L6)  
SODIUM SESQUICARBONATE (UNII: Y1X815621J)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-802-80482 g in 1 CAN; Type 0: Not a Combination Product02/01/2018
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
Accra Pac, Inc.024213616MANUFACTURE(11084-802)

Revised: 12/2020
Document Id: 9058c66b-a0eb-42de-9b6a-eae7c8947d3b
Set id: acc2f83f-6b9b-4552-8330-33e7b99397d8
Version: 2
Effective Time: 20201218
 
SC Johnson Professional USA, Inc.