ALCARE EXTRA HAND SANITIZER- alcohol solution 
SC Johnson Professional USA, Inc.

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Drug Facts

Active ingredient

ETHYL ALCOHOL, 80% w/w

Purpose

Antibacterial

Uses

for hand sanitizing to reduce bacteria on the skin

Warnings

For external use only

Flammable:

Keep away from fire or flame.

When using this product

avoid contact with eyes. In case of eye contact, flush with water.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply foaming sanitizer to cover hands

rub into skin

no rinsing required

Inactive ingredients

AQUA (WATER), BIS-PEG-12 DIMETHICONE, CITRIC ACID, COCO-GLUCOSIDE, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERYL OLEATE, PANTHENOL, PEG-200 HYDROGENATED GLYCERYL PALMITATE, PEG-7 GLYCERYL COCOATE

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

SCJ PROFESSIONAL
HEALTHCARE

Alcare®

NDC 11084-006-27

Hand Sanitizer
Foaming Antiseptic Handrub
Extra

Excellent Moisturization

15
seconds
Fast-acting
CHG Compatible

SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-866-783-0422
Pat. www.scjp.com/patents
www.scjp.com
Made in Canada

1 Liter (33.8 fl oz)
SAP # 400000076
L-1398 R0

REORDER #
101561

deb
SKIN CARE

Open for
Drug Facts

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
ALCARE EXTRA HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
COCO-GLUCOSIDE (UNII: ICS790225B)  
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
GLYCERYL OLEATE (UNII: 4PC054V79P)  
PANTHENOL (UNII: WV9CM0O67Z)  
PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)  
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-006-0147 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2017
2NDC:11084-006-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2017
3NDC:11084-006-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/201712/31/2026
4NDC:11084-006-121000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2017
5NDC:11084-006-661000 mL in 1 BOTTLE; Type 0: Not a Combination Product02/17/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drug505G(a)(3)03/01/2017
Labeler - SC Johnson Professional USA, Inc. (607378015)
Registrant - SC Johnson Professional USA, Inc. (078805627)
Establishment
NameAddressID/FEIBusiness Operations
SC Johnson Professional CA Inc.203765300manufacture(11084-006)

Revised: 12/2024
Document Id: fa751c67-86c2-48d9-aa22-f1ed2b4d7ee8
Set id: b1c8e5d0-a766-4bf0-a385-b7b8940a0e2c
Version: 5
Effective Time: 20241213
 
SC Johnson Professional USA, Inc.