ALCARE PLUS 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® Plus 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), Emulsifying Wax, Hydrofluorocarbon 152A, Isobutane, Polyquaternium-6, Propane, Sodium Benzoate, Sodium Sesquicarbonate

Questions or comments?

1-866-783-0422

PRINCIPAL DISPLAY PANEL - 482 g Can Label

SCJ
PROFESSIONAL
HEALTHCARE

Alcare®

NDC 11084-803-80

Hand Sanitizer
Foamed Antiseptic Handrub

Plus

Excellent Moisturization

15 seconds
Fast Acting

CHG Compatible

Net Weight: 482 g (17 oz)

SAP # 4000000087

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

deb
SKIN CARE

6399-N7H(817)

REORDER #
6399-90

PRINCIPAL DISPLAY PANEL - 482 g Can Label
ALCARE PLUS FOAMED ANTISEPTIC HANDRUB 
alcohol aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-803
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:11084-803-7662.4 g in 1 CAN; Type 0: Not a Combination Product02/01/201806/05/2022
2NDC:11084-803-57153 g in 1 CAN; Type 0: Not a Combination Product02/01/2018
3NDC:11084-803-36255 g in 1 CAN; Type 0: Not a Combination Product02/01/2018
4NDC:11084-803-80482 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(11084-803)

Revised: 12/2020
Document Id: 69fc3e1c-2257-4d33-a7ae-52f98a449f19
Set id: 56900a58-b586-41e5-8b66-c9a006a79a9b
Version: 2
Effective Time: 20201211
 
SC Johnson Professional USA, Inc.