Label: ALCARE ELEVATE ANTISEPTIC HANDRUB- alcohol liquid

  • NDC Code(s): 11084-034-18, 11084-034-27
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Ethyl Alcohol, 70% v/v

  • 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 sanitizer to cover hands
    • rub into skin
    • no rinsing required
  • Inactive ingredients

    Aqua (Water), Glycerin, Hydroxypropyl Cellulose, Panthenol, Parfum (Fragrance), Trisodium Dicarboxymethyl Alaninate.

  • PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

    Alcare®

    Antiseptic Handrub
    Elevate

    SCJ PROFESSIONAL
    HEALTHCARE

    NDC 11084-034-27

    Excellent Moisturization

    Net Contents: 1 Liter (33.8 fl oz)
    SAP # 4000009648

    REORDER #
    ALCELV100

    deb
    SKIN CARE

    PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
  • INGREDIENTS AND APPEARANCE
    ALCARE ELEVATE ANTISEPTIC HANDRUB 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-034
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
    DEXPANTHENOL (UNII: 1O6C93RI7Z)  
    TRISODIUM DICARBOXYMETHYL ALANINATE (UNII: 784K2O81WY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-034-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/15/202012/31/2025
    2NDC:11084-034-18370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/15/202012/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00310/15/202012/31/2025
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Establishment
    NameAddressID/FEIBusiness Operations
    SC Johnson Professional CA Inc.203765300MANUFACTURE(11084-034)
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