Label: CRYSTAL CLEAN INSTANT HAND SANITIZER- ethyl alcohol liquid

  • NDC Code(s): 68041-002-01, 68041-002-02, 68041-002-50
  • Packager: Chemcor Chemical Corporation
  • Category: HUMAN OTC DRUG LABEL

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 January 2, 2023

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  • Drug Facts

  • Active ingredient

    Ethyl alcohol 70% V/V

  • Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Uses •to decrease bacteria on the skin that could cause disease •recommended for repeated use

  • Warnings

    For external use only. Flammable. Keep away from fire or flame

    When using this product •keep out of eyes. In case of contact with eyes, flush thoroughly with water. •avoid contact with broken skin • do not inhale or ingest.

    Stop use and ask a doctor if •irritation or redness develops •condition persists for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

  • DOSAGE & ADMINISTRATION

    Directions •Place enough product on hands to cover all surfaces. Rub hands together until dry. •Supervise children under 6 years of age when using this product to avoid swallowing.

  • STORAGE AND HANDLING

    Other information •Do not store above 105°F •May discolor some fabrics •Harmful to wood finished & Plastics.

  • INACTIVE INGREDIENT

    Inactive ingredients ​​Aminomethyl propanol, Carbomer, Glycerin, Propylene glycol, Water.

  • SPL UNCLASSIFIED SECTION

    KILLS 99.9% OF GERMS

    Fast Drying | Fragrance Free | Kind on hands

    Chemcor Chemical Corporation 13770 Benson Ave., Chino, CA 91710 USA

    1-877-CHEMCOR - www.ChemcorChemical.com

    MADE IN PRC

    24-Hour Chemical Emergency

    Response Number: 1-800-535-5053

  • Packaging

    IMAGEIMAGEIMAGE

  • INGREDIENTS AND APPEARANCE
    CRYSTAL CLEAN INSTANT HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68041-002
    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
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68041-002-013800 mL in 1 BOTTLE; Type 0: Not a Combination Product06/15/2020
    2NDC:68041-002-022000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/15/2020
    3NDC:68041-002-50500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/15/2020
    Labeler - Chemcor Chemical Corporation (018129978)
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