Label: ALCARE EXTRA HAND SANITIZER- alcohol solution

  • NDC Code(s): 11084-006-01, 11084-006-12, 11084-006-27, 11084-006-40
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated March 25, 2021

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  • 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
  • INGREDIENTS AND APPEARANCE
    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 Product03/01/2017
    4NDC:11084-006-121000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/01/2017
    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)
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