Label: SMART CARE GENERIC EMOJI HAND SANITIZER- ethyl alcohol 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 February 16, 2018

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Use To help reduce bacteria and germs on the skin

  • WARNINGS

    Warning Flammable. Keep away from fire or flame. For external use only • Stop use and ask a doctor if irritation or redness develops and persists

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental digestion, seek professional assistance or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    Directions • Place enough product in palm to cover hands and rub hands together briskly until dry • Children under 6, use only under adult supervision • Not recommended for infants.

  • STORAGE AND HANDLING

    Other Information • Do not store above 100o​ F (38o​ C). • M​ay discolor some fabrics • ​Harmful to wood finishes and plastics.

  • INACTIVE INGREDIENT

    Inactive Ingredients ​Water, Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Triethanolamine.

  • SPL UNCLASSIFIED SECTION

    Smart Care

    WWW.SMARTCAREUS.COM

    ONTARIO, CA 91761

    QUESTIONS OR COMMENTS?

    1-877-274-8358 TOLL FREE IN US

    1-909-434-0911 INTERNATIONAL

    DESIGNED IN THE U.S.A

    MANUFACTURED IN CHINA

    COPYRIGHTS AND TRADEMARKS

    GRANTED OR PENDING WORLDWIDE

    DISTRIBUTED BY ASHTEL STUDIOS INC

  • Packaging 

    image description

  • INGREDIENTS AND APPEARANCE
    SMART CARE GENERIC EMOJI HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70108-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70108-011-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product02/02/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/02/2018
    Labeler - Ashtel Studios, Inc. (148689180)
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