Label: ALOE TOUCH- hand sanitizer liquid

  • 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 10, 2017

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  • ACTIVE INGREDIENT

    Active Ingredients - Ethyl Alcohol 70%

  • PURPOSE

    Purpose - Antiseptic

  • INDICATIONS & USAGE

    Use hand sanitizer to help reduce disease causing bacteria on the skin

  • WARNINGS

    Warnings

    Flammable. Keep away from fire or flame

  • INSTRUCTIONS FOR USE

    For external use only -

  • OTHER SAFETY INFORMATION

    Avoid contact with eyes. In case of contact, rinse eyes thoroughly with water

  • STOP USE

    Stop use and ask a doctor if irritation or redeness develops

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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

  • DOSAGE & ADMINISTRATION

    Directions

    • ​Apply liberally to hands and rub thoroughly until dry
    • supervise children in the use of this product
  • INACTIVE INGREDIENT

    Inactive Ingredients

    Water, Carbomer, Triethanolamine, Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice, Fragrance, FD & C Blue# 1, FD & C Yellow# 5

  • PRINCIPAL DISPLAY PANEL

    Hand Sanitizer​SpaSoap

    Hand Sanitizer

    Aloe Touch

    2oz / 59ml

  • INGREDIENTS AND APPEARANCE
    ALOE TOUCH 
    hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71020-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mL  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71020-010-0259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/10/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/10/2017
    Labeler - Sante Manufacturing Inc (242048747)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sante Manufacturing Inc.242048747manufacture(71020-010)
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